Aldehydes
Aldehydes are organic compounds containing a carbonyl group (C=O) bonded to at least one hydrogen atom. These versatile compounds are fundamental in various chemical reactions, including oxidation, reduction, and nucleophilic addition. Aldehydes are essential building blocks in the synthesis of pharmaceuticals, fragrances, and polymers. At CymitQuimica, we provide a diverse selection of high-quality aldehydes to support your research and industrial applications.
Found 8540 products of "Aldehydes"
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1-(3-chlorobenzyl)-1H-indole-3-carbaldehyde
CAS:Formula:C16H12ClNOPurity:95.0%Molecular weight:269.735-chloro-3-(3-methylphenyl)-1,2-oxazole-4-carbaldehyde
CAS:Formula:C11H8ClNO2Purity:95.0%Molecular weight:221.641-(((4-METHOXYBENZYL)OXY)METHYL)CYCLOPROPANE-1-CARBALDEHYDE
CAS:Formula:C13H16O3Purity:95.0%Molecular weight:220.2682-[3-(1H-imidazol-1-yl)propoxy]benzaldehyde hydrochloride
CAS:Formula:C13H15ClN2O2Purity:95.0%Molecular weight:266.735-chloro-3-ethyl-1-(4-fluorophenyl)-1H-pyrazole-4-carbaldehyde
CAS:Formula:C12H10ClFN2OPurity:95.0%Molecular weight:252.673-[(2-chloro-4-fluorobenzyl)oxy]-4-methoxybenzaldehyde
CAS:Formula:C15H12ClFO3Purity:95.0%Molecular weight:294.713-Thiophen-2-yl-benzaldehyde
CAS:Formula:C11H8OSPurity:95%Color and Shape:LiquidMolecular weight:188.245-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)furan-2-carbaldehyde
CAS:Formula:C10H13BO4Purity:98%Molecular weight:208.022-(Dimethylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
CAS:Purity:≥95%Molecular weight:275.16000375-chloro-1-(4-fluorophenyl)-3-propyl-1H-pyrazole-4-carbaldehyde
CAS:Formula:C13H12ClFN2OPurity:95.0%Molecular weight:266.72-(4-Pyridyl)malondialdehyde
CAS:Formula:C8H7NO2Purity:97%Color and Shape:SolidMolecular weight:149.1494-(Benzyloxy)-2,6-difluorobenzaldehyde
CAS:Formula:C14H10F2O2Purity:98%Color and Shape:SolidMolecular weight:248.2292-Fluoro-4-morpholin-4-yl-benzaldehyde
CAS:Formula:C11H12FNO2Purity:95.0%Color and Shape:SolidMolecular weight:209.225-chloro-3-(3-fluorophenyl)-1,2-oxazole-4-carbaldehyde
CAS:Formula:C10H5ClFNO2Purity:95.0%Molecular weight:225.62-Ethoxy-4-formylphenyl isobutyrate
CAS:Formula:C13H16O4Purity:98%Color and Shape:SolidMolecular weight:236.267Tert-butyl 4-(5-formyl-4-methylthiazol-2-yl)piperidine-1-carboxylate
CAS:Purity:95%Molecular weight:310.41000373-Ethoxy-4-methoxybenzaldehyde
CAS:Formula:C10H12O3Purity:98%Color and Shape:SolidMolecular weight:180.2035-chloro-1-(4-fluorophenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde
CAS:Formula:C11H5ClF4N2OPurity:95.0%Molecular weight:292.62Ethyl 3-chloro-4-formylbenzoate
CAS:Formula:C10H9ClO3Purity:98%Color and Shape:SolidMolecular weight:212.631-Boc-4-Formyl-4-methylpiperidine
CAS:Formula:C12H21NO3Purity:98%Color and Shape:LiquidMolecular weight:227.3042-Amino-4-chloro-5-formylthiophene-3-carbonitrile
CAS:Formula:C6H3ClN2OSPurity:98%Molecular weight:186.612,5-Dimethyl-1-pyridin-3-ylmethyl-1H-pyrrole-3-carbaldehyde
CAS:Formula:C13H14N2OPurity:95.0%Color and Shape:SolidMolecular weight:214.2681-isopropyl-1H-imidazole-5-carbaldehyde hydrochloride
CAS:Formula:C7H11ClN2OPurity:95.0%Color and Shape:SolidMolecular weight:174.632-Chloro-4-morpholinopyrimidine-5-carbaldehyde
CAS:Formula:C9H10ClN3O2Purity:95%Molecular weight:227.652′-Fluorobiphenyl-4-carbaldehyde
CAS:Formula:C13H9FOPurity:≥97%Color and Shape:SolidMolecular weight:200.2123′-(Hydroxymethyl)[1,1′-biphenyl]-4-carbaldehyde
CAS:Formula:C14H12O2Purity:97%Molecular weight:212.2484-Formyl-N,N-dimethyl-benzamide
CAS:Formula:C10H11NO2Purity:98%;RGColor and Shape:SolidMolecular weight:177.2033,5-Dimethyl-1-(3-(trifluoromethyl)phenyl)-1H-pyrazole-4-carbaldehyde
CAS:Purity:≥95%Molecular weight:268.23901375-(Benzyloxy)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
CAS:Purity:≥95%Molecular weight:338.20999154-Methoxy-2,5-dimethylbenzaldehyde
CAS:Formula:C10H12O2Purity:95%Color and Shape:SolidMolecular weight:164.2042′-Methoxybiphenyl-4-carboxaldehyde
CAS:Formula:C14H12O2Purity:97%Color and Shape:SolidMolecular weight:212.248tert-Butyl 2-formyl-6,8-dihydro-5H-imidazo[1,2-a]pyrazine-7-carboxylate
CAS:Purity:95+%Molecular weight:251.28599551-isopropyl-1H-pyrrole-3-carbaldehyde
CAS:Formula:C8H11NOPurity:95.0%Color and Shape:LiquidMolecular weight:137.1827-Hydroxy-3,7-dimethyloctanal
CAS:Formula:C10H20O2Purity:95%Color and Shape:Liquid, No data available.Molecular weight:172.2684-Acetyl-1H-pyrrole-2-carbaldehyde
CAS:Formula:C7H7NO2Purity:97%Color and Shape:SolidMolecular weight:137.1383-CHLORO-4-NITROBENZALDEHYDE
CAS:Formula:C7H4ClNO3Purity:95%Color and Shape:Light yellow powderMolecular weight:185.56(3-Bromo-5-formyl-2-methoxyphenyl)boronic acid
CAS:Formula:C8H8BBrO4Purity:96%Molecular weight:258.86Cyclooctanecarbaldehyde hydrate
CAS:Formula:C9H18O2Purity:97.0%Color and Shape:LiquidMolecular weight:158.2413-iso-Propoxybenzaldehyde
CAS:Formula:C10H12O2Purity:97%Color and Shape:LiquidMolecular weight:164.2043-[(DIMETHYLAMINO)METHYL]-5-FLUOROBENZALDEHYDE
CAS:Formula:C10H12FNOPurity:95.0%Molecular weight:181.214-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde
CAS:Formula:C7H4ClN3OPurity:97%Color and Shape:SolidMolecular weight:181.586-Chloro-2,3-difluorobenzaldehyde
CAS:Formula:C7H3ClF2OPurity:98%Color and Shape:Solid, Low-melting solidMolecular weight:176.555-chloro-2-[(2-chloro-4-fluorobenzyl)oxy]benzaldehyde
CAS:Formula:C14H9Cl2FO2Purity:95.0%Molecular weight:299.125-Nitro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
CAS:Purity:98%Molecular weight:277.07998663-Methoxysalicylaldehyde
CAS:Formula:C8H8O3Purity:98%Color and Shape:CrystallineMolecular weight:152.1493′-(Hydroxymethyl)[1,1′-biphenyl]-2-carbaldehyde
CAS:Formula:C14H12O2Purity:95.0%Molecular weight:212.2484-Chloro-2,5-dimethylbenzaldehyde
CAS:Formula:C9H9ClOPurity:≥95%Color and Shape:SolidMolecular weight:168.622-(4-Trifluoromethylphenoxy)-5-nitrobenzaldehyde
CAS:<p>Please enquire for more information about 2-(4-Trifluoromethylphenoxy)-5-nitrobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C14H8F3NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:311.21 g/mol4-(5-(Trifluoromethyl)-2-pyridyl)piperazinecarbaldehyde
CAS:<p>Please enquire for more information about 4-(5-(Trifluoromethyl)-2-pyridyl)piperazinecarbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H12F3N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:259.23 g/mol5-Nitro-2-(2'-pyridinethio)benzaldehyde
CAS:<p>Please enquire for more information about 5-Nitro-2-(2'-pyridinethio)benzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Purity:Min. 95%Cinnamaldehyde thiosemicarbazone
CAS:<p>Cinnamaldehyde thiosemicarbazone is a nitrogen-containing molecule that has been shown to have neuroprotective properties. It is also an antioxidant and potent inhibitor of tyrosinase, which is an enzyme involved in the production of melanin. Cinnamaldehyde thiosemicarbazone has been shown to be effective at nanomolar concentrations in the inhibition of tyrosinase. This compound has been shown to be effective in both basic structure and magnetic resonance spectroscopy studies.</p>Formula:C10H11N3SPurity:Min. 95%Color and Shape:PowderMolecular weight:205.28 g/mol2-(3-Trifluoromethylphenoxy)-5-nitrobenzaldehyde
CAS:<p>Please enquire for more information about 2-(3-Trifluoromethylphenoxy)-5-nitrobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C14H8F3NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:311.21 g/molZolpidem carbaldehyde
CAS:<p>Zolpidem is a sedative-hypnotic drug, which belongs to the class of imidazopyridines. It has a strong affinity for GABA receptors, and can be used as a treatment for insomnia. Zolpidem's chemical structure is similar to that of benzodiazepines. Zolpidem is an acidic compound with a pKa of 3.6. It has been shown to elute from HPLC columns at a hydrodynamic flow rate of 0.5 mL/min on the column of LiChrosorb RP-18e (250 × 4 mm). The optimum pH for chromatographic separation was found to be 4-5. Multiresponse analysis showed statistically significant differences between different batches of zolpidem in terms of particle size, shape and size distribution, surface area and surface charge. Zolpidem carbaldehyde is an organic compound that is used as an intermediate in the production of drugs such as zol</p>Formula:C16H14N2OPurity:Min. 95%Molecular weight:250.3 g/mol4-((4-bromo-2-methyl-5-oxo-1-phenyl(3-pyrazolin-3-yl))methoxy)-3-methoxybenzaldehyde
CAS:<p>Please enquire for more information about 4-((4-bromo-2-methyl-5-oxo-1-phenyl(3-pyrazolin-3-yl))methoxy)-3-methoxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C19H17BrN2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:417.25 g/mol4-((4-methylphenyl)carbonyl)piperazinecarbaldehyde
CAS:<p>Please enquire for more information about 4-((4-methylphenyl)carbonyl)piperazinecarbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Purity:Min. 95%N-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]formamide
CAS:<p>Please enquire for more information about N-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C9H7F4NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:237.15 g/mol4-Piperazin-1-yl-benzaldehyde
CAS:<p>4-Piperazin-1-yl-benzaldehyde (PPBA) is a natural product that has been shown to have effects on animals and cells. PPBA can be used as an antidote for sulfite poisoning, which is caused by the ingestion of sulfites in food or drink. The mechanism of PPBA's effects is not fully known, but it may involve the inhibition of sulfite reductase, which converts sulfites into sulfates. It also reversibly forms a complex with the transition state of the reaction, enhancing the rate of this reaction. This enhancement is due to a low detection limit and shift in solution temperature. PPBA has been shown to have fluorescence and fluorescent properties when exposed to light, making it useful for endogenous labeling.</p>Formula:C11H14N2OPurity:Min. 95%Molecular weight:190.24 g/mol4-(2-propynyloxy)benzenecarboxaldehyde
CAS:<p>4-(2-Propynyloxy)benzenecarboxaldehyde is an organic chemical compound that is classified as a copper complex. This molecule has been shown to have antibacterial properties against P. aeruginosa and other bacteria. It also possesses a constant antibacterial activity in both acidic and neutral pH conditions, which makes it an efficient method of treatment for bacterial infections. 4-(2-Propynyloxy)benzenecarboxaldehyde has been shown to inhibit the growth of P. aeruginosa by binding to the DNA gyrase enzyme and stopping its function, thus inhibiting bacterial replication. 4-(2-Propynyloxy)benzenecarboxaldehyde also inhibits the synthesis of proteins in neuronal cells, which may be due to its ability to react with carbonyl groups in proteins.</p>Purity:Min. 95%2,4,4-Trimethyl-2-pentenal
CAS:Controlled ProductFormula:C8H14OColor and Shape:NeatMolecular weight:126.2(E,E)-5-[4-(Diethylamino)phenyl]penta-2,4-dienal
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications (E,E)-5-[4-(Diethylamino)phenyl]penta-2,4-dienal is used in polymerization process.<br>References Innocenzi, P., et al.: J. Mater Chem., 15, 3821 (2005), Cai, Y., et al.: Polymer, 2006, 47, 6560 (2006),<br></p>Formula:C15H19NOColor and Shape:NeatMolecular weight:229.322,4-Octadienal, predominantly trans,trans (Technical Grade)
CAS:Controlled Product<p>Applications 2,4-Octadienal, predominantly trans,trans >=95%, FG is a useful research chemical for organic synthesis and other chemical processes.<br>References Feng, J., et al.: J. Org. Chem., 82, 1412 (2017); Sun, S., et al.: J. Appl. Phycol., 24, 1003 (2012)<br></p>Formula:C8H12OColor and Shape:NeatMolecular weight:124.18N,N,N-Tributyl-1-butanaminium Salt with (E)-3-Hydroxy-2-propenal
CAS:Controlled Product<p>Applications N,N,N-Tributyl-1-butanaminium Salt with (E)-3-Hydroxy-2-propenal is a useful reagent for preparation of crystalline (±)-fecapentaene.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Pfaendler, H., et al.: J. Am. Chem. Soc., 108, 1338 (1986);<br></p>Formula:C16H36N•CH3O2Color and Shape:Off-WhiteMolecular weight:242.46 + 71.063-(2,4-Dihydroxyphenyl)-2-propenal
CAS:Controlled ProductFormula:C9H8O3Color and Shape:NeatMolecular weight:164.16cis-4-Decenal (>90%)
CAS:Controlled Product<p>Applications CIS-4-DECENAL (cas# 21662-09-9) is a useful research chemical.<br></p>Formula:C10H18OColor and Shape:NeatMolecular weight:154.242-Propyl-2-heptenal (Technical Grade)
CAS:Controlled Product<p>Applications 2-Propyl-2-heptenal is an alkene shown as an metabolic by-product of unsaturated fatty acids metabolism to oxylipins.<br>References Montanari, C., et al.: J. App. Microbiol., 115, 1388 (2013);<br></p>Formula:C10H18OColor and Shape:Clear ColourlessMolecular weight:154.25(2E,4E,6E)-2,4,6-Nonatrienal
CAS:Controlled Product<p>Stability Light Sensitive, Temperature Sensitive<br>Applications (2E,4E,6E)-2,4,6-Nonatrienal is an unsaturated aldehyde that is a natural volatile constituent of aggregation pheromones produced by male flea beetles. (2E,4E,6E)-2,4,6-Nonatrienal is also found in licorice root, one of the widely used herbs for its<br>References Zilkowski, B., et al.: J. Agr. Food Chem., 56, 4982 (2008)<br></p>Formula:C9H12OPurity:>90%Color and Shape:NeatMolecular weight:136.19Oct-7-enal
CAS:Controlled Product<p>Stability Air Sensitive<br>Applications Oct-7-enal is a useful research chemical, an aliphatic aldehyde isolated from the roots of Cirsium Cipsacolepis.<br>References Takano, S., et al.: Phytochemistry, 26, 435 (1987); Halle, M. B., et al.: RSC Adv., 4, 63342 (2014)<br></p>Formula:C8H14OColor and Shape:NeatMolecular weight:126.22-(1H-Pyrazol-1-yl)benzaldehyde
CAS:<p>2-(1H-Pyrazol-1-yl)benzaldehyde is a synthetic chemical compound that is used in the preparation of coupling reactions. It has been shown to be an efficient reagent for the synthesis of 2-bromobenzaldehyde and pyrazole. The molecule has a hydrazone attack, which can be coupled with 2-bromobenzaldehyde, with or without the use of an additional base such as sodium methoxide. This reaction can be carried out at room temperature and does not require any harsh conditions. 2-(1H-Pyrazol-1-yl)benzaldehyde also belongs to the family of aldehydes, which are molecules containing a carbon group that is connected to two hydrogen groups (i.e., RCH=O). Hydrogenation of this type of molecule gives rise to alcohols (RCHOH).</p>Formula:C10H8N2OPurity:Min. 95%Molecular weight:172.18 g/mol2-Hydroxy-4-(trifluoromethyl)benzaldehyde
CAS:<p>2-Hydroxy-4-(trifluoromethyl)benzaldehyde is an analgesic and anti-inflammatory agent that belongs to the pyrazole family. It has shown analgesic and anti-inflammatory effects in animal studies. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been shown to be a potent inhibitor of cyclooxygenase (COX), which is responsible for prostaglandin synthesis, and as such, may have potential as a treatment for inflammatory conditions such as rheumatoid arthritis. This drug also inhibits the production of nitric oxide, which is involved in vasodilation and increased blood flow. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been demonstrated to inhibit COX enzymes by forming a covalent bond with active site serine residues on the enzyme. The docked complex shows hydrogen bonding interactions between the hydroxyl group of 2</p>Formula:C8H5F3O2Purity:Min. 95%Molecular weight:190.12 g/molParaformaldehyde
CAS:<p>Paraformaldehyde is a carcinogenic substance that belongs to the family of heterocyclic compounds. It reacts with water vapor in the air to form formaldehyde, which is responsible for its fluorescence properties. Paraformaldehyde has been used as a probe for DNA and RNA and can be used as an indicator for nonsteroidal anti-inflammatory drugs. The reaction mechanism of paraformaldehyde is not well understood and it has been shown that it reacts with p-hydroxybenzoic acid, polymerase chain, and water vapor. This compound can be found in soybean extract or fetal bovine serum. Paraformaldehyde is usually detected using a plate test or analytical methods such as high performance liquid chromatography (HPLC).</p>Formula:(CH2O)nPurity:90%MinColor and Shape:White Clear LiquidTrans-2-nonenal
CAS:<p>Trans-2-nonenal is a monoclonal antibody that recognizes the physiological function of cardiac and rat liver microsomes. It has been shown to inhibit enzyme activities in both cell lines. Trans-2-nonenal has also been shown to protect against ischemia/reperfusion injury in rats by reducing the release of intracellular Ca2+ and ATP levels. Trans-2-nonenal is genotoxic and induces oxidative injury, which may be due to its ability to react with caproic acid to form reactive oxygen species.</p>Formula:C9H16OPurity:Min. 95%Molecular weight:140.22 g/mol4(5)-Methyl-1H-imidazole-2-carbaldehyde
CAS:<p>Please enquire for more information about 4(5)-Methyl-1H-imidazole-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C5H6N2OPurity:95%NmrMolecular weight:110.11 g/mol2-Chloromalonaldehyde
CAS:<p>2-Chloromalonaldehyde is a reactive chemical that can be used as a pharmaceutical intermediate. It has been shown to have anti-inflammatory properties and is often used in pharmaceutical preparations. 2-Chloromalonaldehyde has shown an ability to bind with integrin receptors and inhibit the production of pro-inflammatory molecules, such as prostaglandins. This compound has also been shown to have a photoelectron spectrum that includes an intramolecular hydrogen bond, which contributes to its biological activity.</p>Formula:C3H3ClO2Purity:(%) Min. 90%Color and Shape:PowderMolecular weight:106.51 g/molp-Anisaldehyde dimethyl acetal
CAS:<p>p-Anisaldehyde dimethyl acetal is a broad-spectrum antimicrobial that can be synthesized from anisaldehyde and dimethoxyacetal. It has been shown to have anticancer properties in vitro. p-Anisaldehyde dimethyl acetal has also been shown to inhibit the growth of HL60 cells, which are specialized white blood cells. This compound was found to increase neuronal death and induce cachexia in mice. The molecular weight of p-Anisaldehyde dimethyl acetal is 244.24 g/mol, with a melting point of -14 °C and a boiling point of 156 °C. The molecule contains one asymmetric center, one hydrogen bond, one non-bonding electron pair, and no double bonds. This compound has acidic properties and it reacts with vitamin D3 in a cationic polymerization process at alkaline pH levels.</p>Formula:C10H14O3Purity:Min. 95%Color and Shape:Colourless To Pale Yellow Clear LiquidMolecular weight:182.22 g/molH-Gly-Phe-Gly-aldehyde semicarbazone acetate salt
CAS:<p>Please enquire for more information about H-Gly-Phe-Gly-aldehyde semicarbazone acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C14H20N6O3Purity:Min. 95%Molecular weight:320.35 g/molBenalaxyl
CAS:<p>Benalaxyl is an insecticide that belongs to the group of organochlorine compounds. It is a chiral compound that has been used in analytical methods for wastewater treatment and as an anti-fouling agent. Benalaxyl has been shown to possess acute toxicity, based on the results of redox cycle experiments, cell nuclei studies, enzyme activities, and rat liver microsomes. Toxicological studies have also shown that benalaxyl can cause high levels of resistance in nutrient solutions, energy metabolism, and synthesis methods.</p>Formula:C20H23NO3Purity:Min. 95%Molecular weight:325.4 g/mol2-Bromo-4-methoxybenzaldehyde
CAS:<p>2-Bromo-4-methoxybenzaldehyde is a cyclic, stereoselectively eliminable, acrylate that can be used in the asymmetric synthesis of sulfamidate and lactam. It can also be used to synthesize quinoline derivatives with aluminium chloride. This product has been shown to yield good yields when reacted with functional groups such as halides and nature. 2-Bromo-4-methoxybenzaldehyde is found in biomolecular reactions.</p>Formula:C8H7BrO2Color and Shape:PowderMolecular weight:215.04 g/molSuccinaldehyde bis(dimethyl acetal)
CAS:<p>Please enquire for more information about Succinaldehyde bis(dimethyl acetal) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C8H18O4Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:178.23 g/mol3,5-Dichloro-4-pyridinecarboxaldehyde
CAS:<p>3,5-Dichloro-4-pyridinecarboxaldehyde is a synthetic heterocycle that has been studied for its pharmacokinetic properties. The compound has the ability to bind to the active site of metalloporphyrin and inhibit the enzyme's activity. This inhibition leads to an increase in the levels of homologous aldehydes, which are oxidized by hydrogen peroxide to produce electrosprays. 3,5-Dichloro-4-pyridinecarboxaldehyde also has a number of oxidation products that have been found in experiments using purines as substrates.</p>Formula:C6H3Cl2NOPurity:Min. 95%Molecular weight:176 g/molDexamethasone-δ17,20 21-aldehyde
CAS:Controlled Product<p>Please enquire for more information about Dexamethasone-δ17,20 21-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C22H27FO4Purity:Min. 95%Color and Shape:PowderMolecular weight:374.45 g/mol3-(Chloromethyl)-4-methoxybenzaldehyde
CAS:<p>3-(Chloromethyl)-4-methoxybenzaldehyde is a natural product that can be extracted from the rhizomes of the plant. It has been shown to have antibacterial activity in laboratory experiments and has been used in traditional medicine for the treatment of fungus infections. 3-(Chloromethyl)-4-methoxybenzaldehyde is an imidazolylmethyl derivative with a hexane structure. It reacts with hydrochloric acid to form a molecule called chloromethylation, which is also known as an esterification reaction. Piperazine acts as a catalyst in this reaction, increasing its scalability and making it suitable for large-scale production. The compound exhibits radical scavenging activity, which may be due to its ability to donate electrons or hydrogen atoms to free radicals.</p>Formula:C9H9CIO2Purity:Min. 95%Molecular weight:288.08 g/mol2-Hydroxy-1-naphthaldehyde
CAS:<p>2-Hydroxy-1-naphthaldehyde is a redox potential chemical that has been shown to have anticancer activity in vitro and in vivo. It inhibits the growth of cells by binding to iron, which is important for many biological processes including DNA synthesis. 2-Hydroxy-1-naphthaldehyde has also been shown to have metal carbonyl reactivity and fluorescence properties that may be useful as a fluorescent probe. 2-Hydroxy-1-naphthaldehyde binds to iron ions through hydrogen bonding interactions, forming an octahedral complex with six ligands. The compound also has coordination geometry that can be described as either trigonal bipyramidal or square planar, depending on the solvent used. This data was obtained by x-ray diffraction studies of crystalline solids. The compound's Langmuir adsorption isotherm was found to be linear at low concentrations and shifted to nonlinear behavior at higher concentrations. The</p>Formula:C11H8O2Purity:Min. 95%Color and Shape:SolidMolecular weight:172.18 g/molTrifluoroacetaldehyde methyl hemiacetal
CAS:<p>Trifluoroacetaldehyde methyl hemiacetal is a chemical compound that inhibits protein synthesis by binding to the ribosomal RNA in microsomes isolated from rat liver. Trifluoroacetaldehyde methyl hemiacetal has been shown to be a bifunctional inhibitor of progesterone receptor, which is an important component of the cell membrane and has been implicated in cancer and bone resorption. Trifluoroacetaldehyde methyl hemiacetal is also effective at inhibiting desflurane-induced anesthesia in rats.</p>Formula:C3H5F3O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:130.07 g/mol2-Furaldehyde diethylacetal
CAS:<p>2-Furaldehyde diethylacetal is a synthetic compound that has been used in the synthesis of calcium carbonate. It is also a potent inhibitor of p. aeruginosa and other bacteria, as well as organic acids and halogen compounds. It reacts with hydroxy groups to form aldehydes, which are then oxidized to form carboxylic acid derivatives. The reaction mechanism for this compound is not well understood, but it is thought that the activation energy for the reaction may be low due to the presence of a furfural functional group.</p>Formula:C9H14O3Purity:Min. 95%Molecular weight:170.21 g/molSuccinicsemialdehyde
CAS:<p>Succinicsemialdehyde is a semialdehyde that is formed by the oxidative degradation of succinic acid. Succinicsemialdehyde has been shown to have high affinity for 5-HT3 receptors, which are found in the gastrointestinal tract and are involved in intestinal motility and bowel disease. The 5-HT3 receptor has been shown to be an important target for the treatment of irritable bowel syndrome. This semialdehyde also inhibits polymerase chain reaction (PCR) activity, which may be due to its ability to inhibit DNA synthesis. Succinicsemialdehyde has been shown to inhibit enzymes involved in energy metabolism, such as glutamate dehydrogenase and pyruvate formate lyase. The structural analysis of this molecule shows a keto group at C2, which indicates that it is a keto acid.</p>Formula:C4H6O3Purity:Min. 95%Color and Shape:PowderMolecular weight:102.09 g/mol5-(Methoxymethyl)-2-furancarboxaldehyde
CAS:<p>5-hydroxymethylfurfural (5-hmf) is an organic compound that is produced when a carbohydrate or sugar undergoes oxidation. It is used as an additive in animal feed and as an industrial chemical. 5-hmf is a solid catalyst that can be used at high temperatures, making it suitable for use in the production of 2,6-dihydroxybenzoic acid. The reaction mechanism of 5-hmf involves the dehydration of furfural to form 5-hydroxymethylfurfural. This process occurs when a molecule of water reacts with furfural to produce two molecules of 5-hmf. The reaction may be accelerated by introducing heat, which breaks down the hydrogen bonds between the molecules of furfural and water.</p>Formula:C7H8O3Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:140.14 g/mol4-Bromobenzaldehyde
CAS:<p>Please enquire for more information about 4-Bromobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C7H5BrOMolecular weight:185.03 g/molN-Methyl-N-hydroxyethyl-4-aminobenzaldehyde
CAS:<p>N-Methyl-N-hydroxyethyl-4-aminobenzaldehyde (NHABA) is a bathochromic molecule that absorbs light at wavelengths of 400 to 500 nm. It is reactive and reacts with metal cations to form chromophores. NHABA has been shown to be a fluorescent probe for the detection of tyrosinase and autophagy in human serum. It also has inhibitory properties against tyrosinase, which may be due to its ability to inhibit the formation of melanin. NHABA is used as an analytical chemistry reagent for the determination of ammonia, nitrite, and nitrate ions in water samples. This molecule can also be used as a chemosensor for the detection of phenolic compounds in water samples.</p>Formula:C10H13NO2Purity:Min. 95%Molecular weight:179.22 g/mol3,4-Dichlorobenzaldehyde
CAS:<p>3,4-Dichlorobenzaldehyde is a monosubstituted aromatic organic compound with inhibitory effects. 3,4-Dichlorobenzaldehyde has shown significant antifungal activity against Candida albicans and Saccharomyces cerevisiae. It also inhibits the growth of certain cancer cells in cell culture studies. 3,4-Dichlorobenzaldehyde has been found to have anti-inflammatory properties and would be effective in treating inflammatory diseases such as asthma or arthritis. This compound has been shown to have significant effects on energy metabolism and fatty acid synthesis by inhibiting enzymes that are involved in these processes. 3,4-Dichlorobenzaldehyde can also be used to treat metabolic disorders such as diabetes mellitus type II and hyperlipidemia by inhibiting enzymes that are involved in these processes.</p>Formula:C7H4Cl2OPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:175.01 g/mol2-Phenoxyacetaldehyde
CAS:<p>2-Phenoxyacetaldehyde is a reactive molecule that has been shown to inhibit the growth of hematopoietic cells. It also inhibits the production of active enzymes, such as amylase, by interfering with the nucleophilic attack and oxidation of 2-phenoxyacetaldehyde. The synthesis methods for 2-phenoxyacetaldehyde include homogeneous catalysts and chemical reactions. This molecule has been used in detergent compositions, but it is not suitable for use in food contact materials because of its toxicity.</p>Formula:C8H8O2Purity:Min. 95%Molecular weight:136.15 g/molHeptaldehyde
CAS:<p>Heptaldehyde is a colorless liquid with a pleasant, sweet odor. It is used in the production of polyvinyl chloride and other chemicals. In addition, it can be an important biomarker in environmental studies. Heptaldehyde is produced by the reaction of ethyl decanoate with water vapor or methyl ethyl ketone. It is also an inhibitor of acetylcholinesterase, which may be due to its hydroxyl group and acetyl group. Furthermore, heptaldehyde has been shown to react with p-nitrophenyl phosphate to form p-nitrophenol. The following table outlines the chemical properties of heptaldehyde: Molecular formula: C7H8O Molecular weight: 112.14 g/mol Boiling point (°C): 212 °C Melting point (°C): -78 °C Density (g/cm3): 1.096</p>Formula:C7H14OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:114.19 g/mol4-Cinnolinecarboxaldehyde
CAS:<p>4-Cinnolinecarboxaldehyde is an organic compound that belongs to the group of cinnoline. It is a colorless liquid that can be used as a precursor in the production of aluminum metal. 4-Cinnolinecarboxaldehyde reacts with lithium aluminum hydride to form a compound that can be used as a reducing agent in organic chemistry. 4-Cinnolinecarboxaldehyde is also used as a precursor for preparing other compounds, such as lithium aluminum hydride and lithium aluminum trihydride.</p>Formula:C9H6N2OPurity:Min. 95%Molecular weight:158.16 g/mol2-Hydroxy-3-(Trifluoromethoxy)Benzaldehyde
CAS:<p>2-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a coordination compound that is used as a ligand. It has two-dimensional and crystal structures. The ligated molecule is usually coordinated to the metal ion, forming a dimer.</p>Formula:C8H5F3O3Purity:Min. 95%Molecular weight:206.12 g/mol5-Bromo-3-methoxybenzaldehyde
CAS:<p>5-Bromo-3-methoxybenzaldehyde is a type of growth factor that is synthesized by cancer cells. It has been shown to have anticancer activity when used in conjunction with other drugs. 5-Bromo-3-methoxybenzaldehyde has been shown to inhibit tumor growth in mice, which may be due to its ability to prevent the activation of PD-L1. This compound interacts with a tetranuclear ligand and can be activated by light.</p>Formula:C8H7BrO2Purity:Min. 95%Color and Shape:PowderMolecular weight:215.04 g/molValiphenal
CAS:<p>Valiphenal is a chemical compound that belongs to the amide class. It has been shown to control the growth of various bacterial strains, such as Escherichia coli and Salmonella enterica serovar Typhimurium. Valiphenal inhibits lipid biosynthesis in bacteria by binding to bacterial matrix effect enzymes, which are involved in fatty acid synthesis. This inhibition leads to a decrease in the production of lipids, which are an important component of bacterial cell membranes. Valiphenal also inhibits mitochondrial cytochrome c oxidase and can be used as an analytical tool for determining the presence of this enzyme in cells. Valiphenal is also used as an agrochemical to control pests on vegetables such as aubergines. Valiphenal is extensively metabolized by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>Formula:C19H27ClN2O5Purity:Min. 98 Area-%Color and Shape:White Clear LiquidMolecular weight:398.88 g/mol4-Ethylbenzaldehyde
CAS:<p>4-Ethylbenzaldehyde is a chemical compound that belongs to the group of fatty acids. It has been shown to have biological properties, such as antiviral potency and genotoxic effects. This chemical compound also has a gas sensor property and is used as an exothermic reactant in organic synthesis reactions. 4-Ethylbenzaldehyde has been shown to inhibit the growth of bacteria, fungi, and viruses by blocking the synthesis of viral nucleic acid or inhibiting viral protein synthesis. The magnetic resonance spectroscopy (NMR) spectral data for 4-ethylbenzaldehyde show that this chemical compound contains two methyl groups, one on each side of the benzene ring, with a hydroxyl group on one end. The carbon atoms are bonded together in an alternating pattern of single and double bonds. The molecular formula for 4-ethylbenzaldehyde is C9H10O2.</p>Formula:C9H10OPurity:Min. 96.0%Color and Shape:PowderMolecular weight:134.18 g/mol2-O-Tolyl-thiazole-4-carbaldehyde
CAS:<p>Please enquire for more information about 2-O-Tolyl-thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H9NOSPurity:Min. 95%Molecular weight:203.26 g/mol4-tert-Butylbenzaldehyde
CAS:<p>4-tert-Butylbenzaldehyde is an organic compound with the molecular formula CH3COCH2C6H5. It is a viscous liquid that is insoluble in water and has a boiling point of 146 °C. 4-tert-Butylbenzaldehyde reacts with cationic surfactants to form polymeric micelles, which are spherical structures composed of many small spherical subunits. These polymeric micelles are used as model systems for studying the properties of surfactant aggregates in solution. The reaction mechanism for this polymerization process involves the oxidation of 4-tert-butylbenzaldehyde by hydrogen peroxide and the subsequent condensation of 4-tert-butylbenzoic acid with malonic acid or other cinnamic acid derivatives to form the corresponding esters. The oxidized product, 4-tert-butylbenzoic acid, can be regenerated by boiling a mixture containing it</p>Formula:C11H14OPurity:Min. 96.5%Color and Shape:Colorless Clear LiquidMolecular weight:162.23 g/mol1-Methyl-2-imidazolecarboxaldehyde
CAS:<p>1-Methyl-2-imidazolecarboxaldehyde is a compound that has been studied for its redox potential, which is the measure of the tendency of a molecule to gain or lose electrons. 1-Methyl-2-imidazolecarboxaldehyde has shown to be an excellent candidate as an electrochemical probe. The molecule has also been shown to bind chloride ions in water, forming a tetradentate chelate ring. This type of chelate ring is formed between two nitrogen atoms and four oxygen atoms from the water molecule. The compound forms hydrogen bonds with other molecules in its vicinity, including hepg2 cells and chloride ions.</p>Formula:C5H6N2OPurity:Min. 95%Color and Shape:White To Yellow To Orange Solid Or Liquid (May Vary)Molecular weight:110.11 g/mol5-(1H-Pyrazol-5-yl)thiophene-2-carbaldehyde
CAS:<p>Please enquire for more information about 5-(1H-Pyrazol-5-yl)thiophene-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C8H6N2OSPurity:Min. 95%Molecular weight:178.21 g/molFormaldehyde-d2 solution, 20 wt. % in D2O
CAS:Controlled Product<p>Formaldehyde-d2 solution is a formaldehyde solution that contains deuterium, which has the same chemical properties as hydrogen but has an additional neutron in its nucleus. Formaldehyde-d2 solution is used to prepare samples for NMR and ESI-MS experiments. The reaction mechanism of formaldehyde is believed to be an acid-catalyzed hydrolysis of the hydrogen bond between formaldehyde and methanol. Deuterium isotopes are generally considered to be non-radioactive and have little or no effect on biological systems. Formaldehyde-d2 solution can inhibit fatty acids from binding to the surface of potatoes, which may make it useful in treating autoimmune diseases.</p>Formula:CD2OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:32.04 g/mol4-Bromo-2-hydroxybenzaldehyde
CAS:<p>4-Bromo-2-hydroxybenzaldehyde is a versatile building block that can be used as a reaction component to synthesize other compounds. 4-Bromo-2-hydroxybenzaldehyde is a useful intermediate in the manufacture of pharmaceuticals, pesticides, and herbicides. This chemical also has various applications in research and industry. It is an important reagent for the production of polymers and resins, as well as being an essential raw material for the synthesis of pharmaceuticals and agrochemicals.</p>Formula:C7H5BrO2Molecular weight:201.02 g/molRef: 3D-W-201939
25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-ggTo inquire2-Methylbut-2-enal
CAS:<p>2-Methylbut-2-enal is an aldehyde that belongs to the class of fatty acid. It has been shown that 2-methylbut-2-enal inhibits the growth of bacteria by binding to the anhydrous sodium and tiglic acid in the bacterial cell wall. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. 2-Methylbut-2-enal also inhibits locomotor activity in mice, which may be due to its ability to inhibit acetylcholinesterase.</p>Formula:C5H8OPurity:Min. 95%Molecular weight:84.12 g/mol2-fluoro-5-hydroxybenzaldehyde
CAS:<p>2-Fluoro-5-hydroxybenzaldehyde (2FHBA) is an olefinic compound that is synthesized from 2,5-dihydroxybenzaldehyde by reductive amination with formaldehyde. The configuration of 2FHBA is dependent on the dihedral angle between the two olefinic groups. Liquid chromatography has been used to analyze the metabolic pathway of 2FHBA in rats and humans. This study showed that tyramine and aligned are metabolites of 2FHBA in rats, while crystallized and emission are metabolites in humans. The positron emission studies also showed that 2FHBA was metabolized by erythrocytes in vitro to produce positron emission.</p>Formula:C7H5FO2Purity:Min. 95%Molecular weight:140.11 g/molAdrenalone
CAS:Controlled Product<p>Adrenalone is a caffeic acid derivative that contains a hydroxyl group. It is used in the treatment of infectious diseases, bowel disease, and autoimmune diseases. Adrenalone inhibits bacterial growth by interfering with cell wall synthesis, which prevents the formation of new cell walls and leads to bacterial death. It also inhibits the production of dopamine by acting on an amine oxidase enzyme. This drug has been shown to be effective in treating inflammatory bowel disease (IBD) in both mice and humans due to its ability to inhibit pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6.</p>Formula:C9H11NO3Purity:Min. 95%Color and Shape:Colourless To Pale Yellow SolidMolecular weight:181.19 g/mol2-Cyanobenzaldehyde
CAS:<p>2-Cyanobenzaldehyde is an aldehyde that reacts with nucleophiles such as trifluoromethanesulfonic acid to form a molecule. 2-Cyanobenzaldehyde has potent inhibitory activity against the kinase glycogen synthase kinase 3 (GSK3) and can be used to treat autoimmune diseases. It also reacts with hydrochloric acid in solution to form an intermediate, which is then reacted with glycine and ATP to produce a chiral compound. The product of this reaction has been shown to be active methylene, which was synthesized by asymmetric synthesis.</p>Formula:C8H5NOPurity:Min. 95%Color and Shape:PowderMolecular weight:131.13 g/mol2-Fluoro-4-hydroxybenzaldehyde
CAS:<p>2-Fluoro-4-hydroxybenzaldehyde is an oxidative compound that is a model compound of phenolic compounds. It can be used to synthesize 2,6-dichloroquinone and 2,5,7,8-tetrachlorodibenzo[p]fluoranthene. The metabolic pathway for this compound starts with the oxidative decarboxylation of L-tyrosine to form 4-hydroxyphenylpyruvic acid. This compound is then oxidized by cytochrome P450 enzymes to form 4-(2'-oxo)phenol. The 4-(2'-oxo)phenol can be methylated by S-adenosylmethionine in order to form 2-fluoro-4-hydroxybenzaldehyde.</p>Formula:C7H5FO2Purity:Min. 95%Molecular weight:140.11 g/mol1-Phenyl-1H-pyrazole-4-carbaldehyde
CAS:<p>1-Phenyl-1H-pyrazole-4-carbaldehyde is an antibacterial agent that has been shown to have bactericidal activity against bacteria. It inhibits the growth of bacteria by binding to the pyrazole ring in the bacterial cell wall and blocking the formation of a hydrogen bond. 1-Phenyl-1H-pyrazole-4-carbaldehyde has been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Ciprofloxacin resistant Pseudomonas aeruginosa isolates, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>Formula:C10H8N2OPurity:Min. 95%Molecular weight:172.18 g/mol2,4-Dihydroxy-6-methylbenzaldehyde
CAS:<p>2,4-Dihydroxy-6-methylbenzaldehyde is a chemical that is found naturally in a variety of plants. It has been shown to have immunomodulatory and anti-inflammatory effects in vitro and in vivo. 2,4-Dihydroxy-6-methylbenzaldehyde has been shown to reduce the production of inflammatory molecules such as tumor necrosis factor alpha (TNFα) and interleukin 12 (IL-12) by inhibiting the activation of microglia cells. This compound also inhibits LPS induced inflammatory response in human carcinoma cells. 2,4-Dihydroxy-6 methylbenzaldehyde is currently undergoing clinical trials for its potential use in regenerative medicine.</p>Formula:C8H8O3Purity:Min. 95%Molecular weight:152.15 g/mol4-(Benzyloxy)-5-methoxy-2-nitrobenzaldehyde
CAS:<p>4-(Benzyloxy)-5-methoxy-2-nitrobenzaldehyde (BOMBA) is an amide with affinity for microtubules. It has been shown to interact with the microtubule lattice and inhibit the polymerization of tubulin. This leads to a decrease in cell viability and cytotoxicity, as well as a decrease in tumor size. In vivo studies have demonstrated that BOMBA inhibits tumor growth by inducing thrombosis and coagulation, which results in reduced blood flow to the tumor. The mechanism of action of BOMBA is thought to be due to its ability to form sulfamates, which are known for their anti-coagulant activity.</p>Formula:C15H13NO5Purity:Min. 95%Molecular weight:287.27 g/molTetrafluoroterephthaldehyde
CAS:<p>Tetrafluoroterephthaldehyde (TFPA) is a reactive aldehyde that can be synthesized in the laboratory by the reaction of trifluoromethanesulfonic acid with an aromatic hydrocarbon or ester compound. TFPA has been used to study the synthesis of supramolecular assemblies and supramolecular chemistry. The radiation-induced formation of TFPA is a useful method for the synthesis of polymers, and the thermal expansion of TFPA is high enough to be used as a thermometer. TFPA has shown chemical stability in both acidic and alkaline media, as well as resistance to radiation and oxidation. TFPA also has a high boiling point, making it useful for desolvation during gas chromatography experiments.</p>Formula:C8H2F4O2Purity:Min. 95%Color and Shape:PowderMolecular weight:206.09 g/mol(R)-Perillaldehyde
CAS:<p>(R)-Perillaldehyde is an activated cardenolide that binds to flavoproteins and inhibits the oxygenation of 4-hydroxycoumarin. It is a stereoselective, substrate binding, and oxygenated flavoenzyme inhibitor. The orientation of perillaldehyde with respect to the flavin may be important for its activity in the enzyme's active site.</p>Formula:C10H14OPurity:Min. 95%Molecular weight:150.22 g/molButyraldehyde
CAS:<p>Butyraldehyde is a colorless to yellowish liquid with a strong, pungent odor. It is soluble in water and has an acidic pH of 2.6-3.0. Butyraldehyde is used as a chemical intermediate for the production of polyvinyl acetate and can be made by reacting acetic acid with butanol or butyl acetate. This chemical reacts with human serum albumin at low concentrations and may have biological properties such as catalyzing the conversion of picolinic acid to nicotinic acid, which aids in the prevention against infectious diseases. Butyraldehyde also has synergistic effects when used with picolinic acid, increasing its effectiveness in combating infection.</p>Formula:C4H8OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:72.11 g/mol4-(Dimethylamino)-2-hydroxybenzaldehyde
CAS:<p>4-(Dimethylamino)-2-hydroxybenzaldehyde (DMAA) is an anticancer agent that has been shown to enhance the antitumor effect of sodium succinate. DMAA binds to the tetradentate site of the DNA and prevents it from binding with a transcription factor, which may lead to cancer cell death. DMAA has low detection in urine and blood, making it difficult to detect its presence in patients. DMAA also has no known complexation partners, making it difficult for the body to excrete this drug. DMAA is not carcinogenic or mutagenic. It is used as a fluorescent probe for detecting hydroxy groups in organic compounds and as an environmental pollutant when mixed with other chemicals such as benzene and methylene chloride.</p>Purity:Min. 95%Adrenalone hydrochloride
CAS:Controlled Product<p>Adrenalone hydrochloride is a synthetic form of epinephrine, which is an endogenous catecholamine. Adrenalone hydrochloride has been used to treat autoimmune diseases and bowel disease. Adrenalone hydrochloride binds to the alpha and beta receptors on the surface of cells, which stimulates the production of other hormones and neurotransmitters. It has also been shown to have antimicrobial properties against bacteria, fungi, and viruses. Adrenalone hydrochloride has a chemical stability that is greater than that of dopamine or adrenaline.</p>Formula:C9H11NO3·HClPurity:Min. 95%Molecular weight:217.65 g/mol5,6,7,8-Tetrahydronaphthalene-1-carbaldehyde
CAS:<p>Please enquire for more information about 5,6,7,8-Tetrahydronaphthalene-1-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H12OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:160.21 g/mol4-Nitro lenalidomide
CAS:<p>4-Nitro lenalidomide is an organic compound that is a derivative of the drug lenalidomide. It is synthesized by reacting 2-nitrobenzaldehyde with amines, yielding 4-nitro-N-(2-chloroethyl)-N-(2,3-dihydroxypropyl)benzamide or 4-nitrolenalidomide. This reaction occurs in tetrahydrofuran (THF) as a solvent and in the presence of sodium borohydride (NaBH4). The four nitro groups are used to control the enantiomeric purity of the product. The chemical formula for 4-nitro lenalidomide is C12H14ClNO2.</p>Formula:C13H11N3O5Purity:Min. 95%Molecular weight:289.24 g/mol1,2,4,5-Tetramethyl-1H-pyrrole-3-carbaldehyde
CAS:<p>Please enquire for more information about 1,2,4,5-Tetramethyl-1H-pyrrole-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C9H13NOPurity:Min. 95%Molecular weight:151.21 g/mol3,5,3',5'-Tetraiodo thyroaldehyde
CAS:<p>Please enquire for more information about 3,5,3',5'-Tetraiodo thyroaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C13H6I4O3Purity:Min. 95%Color and Shape:PowderMolecular weight:717.8 g/mol
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