Building Blocks
Questa sezione contiene prodotti fondamentali per la sintesi di composti organici e biologici. Building blocks sono i materiali di partenza essenziali utilizzati per costruire molecole complesse attraverso varie reazioni chimiche. Svolgono un ruolo critico nella scoperta di farmaci, nella scienza dei materiali e nella ricerca chimica. Presso CymitQuimica, offriamo una gamma diversificata di building blocks di alta qualità per supportare le tue ricerche innovative e progetti industriali, assicurandoti di avere i componenti essenziali per una sintesi di successo.
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.756 prodotti)
- Building Blocks Chirali(1.242 prodotti)
- Building Blocks Idrocarburici(6.093 prodotti)
- Building Blocks organici(60.525 prodotti)
Trovati 195536 prodotti di "Building Blocks"
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7,8-Dimethylquinoline
CAS:<p>7,8-Dimethylquinoline is an electrophilic agent that has been shown to be active against a variety of fungi. 7,8-Dimethylquinoline is a phenolic compound that can be used as an antifungal agent and has been shown to possess narcotic properties. 7,8-Dimethylquionline is not toxic to mammals but may cause toxicity in other organisms. It also has potential to inhibit membrane transport processes in fungi.</p>Formula:C11H11NPurezza:Min. 95%Peso molecolare:157.22 g/molMethyl 2-Acetamido-5-chlorobenzoate
CAS:<p>Methyl 2-acetamido-5-chlorobenzoate is a chemical compound that belongs to the group of organic compounds. It has a crystal structure with orthorhombic and isotropic properties. The radiation used in the measurement of this compound is atomic and it has been measured using a Bruker instrument.</p>Formula:C10H10ClNO3Purezza:Min. 95%Peso molecolare:227.64 g/molRef: 3D-VAA67654
25gPrezzo su richiesta50gPrezzo su richiesta100gPrezzo su richiesta250gPrezzo su richiesta500gPrezzo su richiesta250mg348,00€2500mg1.299,00€1-(2-Chloroethyl)-3,5-dimethylcyclohexane
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H19ClPurezza:Min. 95%Peso molecolare:174.71 g/mol1-Methyl-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H13NOPurezza:Min. 95%Peso molecolare:175.23 g/mol1-(4-Bromophenyl)-3-methylurea
CAS:<p>1-(4-Bromophenyl)-3-methylurea is a nitrosourea that has been shown to be carcinogenic in experiments. It is an alkylating agent that may also have genotoxic properties. 1-(4-Bromophenyl)-3-methylurea can react with DNA, forming DNA adducts. This chemical is a potent inhibitor of the enzyme nitrite reductase, which reduces nitrite to nitric oxide and water. Nitric oxide is important for blood vessel dilation and vasodilation, as well as the regulation of vasoconstriction. The inhibition of this enzyme leads to increased blood pressure by blocking these effects. 1-(4-Bromophenyl)-3-methylurea is commonly used in the laboratory to induce papillomas on the skin of animals or fish, as well as carcinogenic activity in vitro.</p>Formula:C8H9BrN2OPurezza:Min. 95%Peso molecolare:229.07 g/molRef: 3D-VAA68007
1mgPrezzo su richiesta250mg298,00€50µgPrezzo su richiesta100µgPrezzo su richiesta2500mg1.126,00€250µgPrezzo su richiesta500µgPrezzo su richiestaPropane-1,3-disulfonyl dichloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C3H6Cl2O4S2Purezza:Min. 95%Peso molecolare:241.1 g/molN-(Cyclohexylmethyl)-2-hydroxyacetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H17NO2Purezza:Min. 95%Peso molecolare:171.24 g/mol1-[(4-Fluorophenyl)methyl]cyclohexane-1-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H17FO2Purezza:Min. 95%Peso molecolare:236.28 g/mol1-[(4-Methylphenyl)methyl]cyclohexane-1-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C15H20O2Purezza:Min. 95%Peso molecolare:232.32 g/mol2-{Bicyclo[2.2.1]heptan-2-yl}ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H16OPurezza:Min. 95%Peso molecolare:140.22 g/mol[2-(2-Chlorophenoxy)ethyl](methyl)amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H12ClNOPurezza:Min. 95%Peso molecolare:185.65 g/mol1,2,3-Tripentyl 2-hydroxypropane-1,2,3-tricarboxylate
CAS:<p>1,2,3-Tripentyl 2-hydroxypropane-1,2,3-tricarboxylate (TPTC) is a citric acid derivative that has been shown to have antibacterial activity. It is used in the production of coatings and as an intermediate in the manufacture of cellulose acetate. TPTC can be synthesized by reacting orthophosphoric acid with 1,2,3-tripentyl 2-bromopropane-1,2,3-tricarboxylate. TPTC has a reaction rate that is faster than that of the corresponding ester derived from glycerol or sorbitol. This makes it suitable for use in coatings manufacturing and other applications where processability is important.</p>Formula:C21H38O7Purezza:Min. 95%Peso molecolare:402.5 g/molCyclopropyl (4-bromophenyl)methanol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11BrOPurezza:Min. 95%Peso molecolare:227.1 g/mol2,2-Dimethyl-N-pyridin-3-yl-propionamide
CAS:<p>2,2-Dimethyl-N-pyridin-3-yl-propionamide is a tertiary amide with a pyridine ring that forms a dimer. It is soluble in water and has no odor or taste. 2,2-Dimethyl-N-pyridin-3-yl-propionamide has two orientations and hydrogen bonds occur between the tertiary amide groups. There are also two carbonyls in this compound, which are C=O groups. The crystal structure of 2,2-Dimethyl-N-pyridin3ylpropionamide is disordered because it does not have any long range order.</p>Formula:C10H14N2OPurezza:Min. 95%Peso molecolare:178.23 g/mol2,2-Dimethyl-N-pyridin-4-yl-propionamide
CAS:<p>2,2-Dimethyl-N-pyridin-4-yl-propionamide is an analgesic and antipyretic drug with anti-inflammatory properties. It has been shown to inhibit the synthesis of prostaglandins, which are important mediators of inflammation. This disulphide compound is synthesized by reacting 2,2-dimethylpyridine with propionic acid chloride in the presence of a base such as pyridine. The product can be hydrolyzed to phenothiazines, which are drugs with antipsychotic effects.</p>Formula:C10H14N2OPurezza:Min. 95%Peso molecolare:178.24 g/mol2-{[(Furan-2-ylmethyl)amino]methyl}phenol
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13NO2Purezza:Min. 95%Peso molecolare:203.24 g/mol3-Phenyl-3,4-dihydro-2H-1,4-benzoxazine
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H13NOPurezza:Min. 95%Peso molecolare:211.26 g/mol4-Hydroxy-5-nitrobenzene-1,3-dicarbaldehyde
CAS:<p>4-Hydroxy-5-nitrobenzene-1,3-dicarbaldehyde (HNAD) is a formyl group that is used as a reagent in organic synthesis. It reacts with phosphonium salts to give formylphosphonium salts. HNAD has been shown to be an excellent chromophore for the bathochromic shift and fluorescence techniques. This compound has also been used in the Wittig reaction, which is a method of synthesizing substituted phenols from olefins and phenols. HNAD can also be used to synthesize chromenes via the wittig reaction and uv irradiation.</p>Formula:C8H5NO5Purezza:Min. 95%Peso molecolare:195.13 g/mol1-{6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl}ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H7ClN2OSPurezza:Min. 95%Peso molecolare:202.66 g/mol(2E)-3-(5-methylthiophen-2-yl)prop-2-enoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H8O2SPurezza:Min. 95%Peso molecolare:168.21 g/mol2-Methyl-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H14O2Purezza:Min. 95%Peso molecolare:190.24 g/mol3-Chloro-1-(4-fluorophenyl)butan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10ClFOPurezza:Min. 95%Peso molecolare:200.64 g/mol4,6-Dimethylpyrimidin-5-ol
CAS:<p>4,6-Dimethylpyrimidin-5-ol (4,6-DMP) is a small molecule that is an immunomodulatory agent. It has been shown to have immunomodulatory effects on cells in vitro and in vivo. 4,6-DMP binds to the lipid bilayer of cell membranes and inhibits the activity of phosphoinositide 3-kinase, which results in changes in the intracellular concentration of calcium ions. This leads to an increase in cytokine production by T cells and B cells, as well as an increase in IgG production by plasma cells. Kinetic constants for the reactions of 4,6-DMP with various chemical moieties have been reported. These constants are useful for determining rates of reaction with other chemicals and can be used to determine mechanisms for 4,6-DMP’s antitumor activity.</p>Formula:C6H8N2OPurezza:Min. 95%Peso molecolare:124.14 g/mol(2E)-3-(1-Methyl-1H-imidazol-5-yl)prop-2-enoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8N2O2Purezza:Min. 95%Peso molecolare:152.15 g/mol2-N-(4-Methylphenyl)pyridine-2,3-diamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13N3Purezza:Min. 95%Peso molecolare:199.25 g/mol4,4,7-Trimethyl-1,2,3,4-tetrahydronaphthalen-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H16OPurezza:Min. 95%Peso molecolare:188.26 g/mol2-[2-(1-Methyl-1H-indol-3-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C19H16N2O2Purezza:Min. 95%Peso molecolare:304.3 g/mol5-Amino-1,3-dimethyl-1H,2H,3H,4H-[1,3]diazino[4,5-d]pyrimidine-2,4-dione
CAS:<p>Azelastine belongs to the class of antihistamines, and is used in the treatment of allergic diseases. It inhibits histamine release from mast cells and basophils, which are white blood cells responsible for inflammatory reactions, such as asthma and allergic rhinitis. Azelastine is not active against infections, but it is effective in the treatment of conjunctivitis caused by allergies or infection. Azelastine also has a local anesthetic effect on the eye. This drug is available in a nasal spray that can be used to treat allergic rhinitis, conjunctivitis and dermatopathy.br><br>Azelastine has been shown to inhibit the growth of bacteria that are resistant to penicillin, ampicillin, erythromycin. Azelastine binds to the penicillin-binding proteins in the bacterial cell wall by competitive inhibition. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis</p>Formula:C8H9N5O2Purezza:Min. 95%Peso molecolare:207.19 g/mol5-Amino-1-phenyl-2,3-dihydro-1H-pyrazol-3-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H9N3OPurezza:Min. 95%Peso molecolare:175.19 g/mol5-Chloro-3-(N-methylsulfamoyl)thiophene-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H6ClNO4S2Purezza:Min. 95%Peso molecolare:255.7 g/mol2,5-Dibromothiophene-3-sulfonyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C4HBr2ClO2S2Purezza:Min. 95%Peso molecolare:340.4 g/mol(S)-1-(Methylamino)-2-propanol Hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H11NO·HClPurezza:Min. 95%Peso molecolare:125.59 g/mol1-Benzyl-4-(bromomethyl)-1H-1,2,3-triazole
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10BrN3Purezza:Min. 95%Peso molecolare:252.11 g/mol5-(2-Thienyl)-1,3-oxazole
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H5NOSPurezza:Min. 95%Peso molecolare:151.19 g/mol4-(1,3-Oxazol-5-yl)pyridine
CAS:<p>4-(1,3-Oxazol-5-yl)pyridine (4-OP) is an organic solvent that is also a bioisoster of nicotinic acid and nicotinamide. It has significant activity against some bacteria and fungi, and can be used as an antimicrobial agent. 4-OP is decarboxylated by alkali metal hydroxides to give the corresponding amine salt. This process yields a high yield of 4-OP, which can be purified via column chromatography or crystallization with aqueous ammonia. 4-OP has been shown to inhibit streptochlorin production in Streptomyces clavuligerus and act as an antibiotic against Escherichia coli and Pseudomonas aeruginosa.</p>Formula:C8H6N2OPurezza:Min. 95%Peso molecolare:146.15 g/mol3-Benzyl-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C16H14N2O2Purezza:Min. 95%Peso molecolare:266.29 g/mol6-Amino-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H7N5OPurezza:Min. 95%Peso molecolare:165.15 g/mol2-(Chloromethyl)-5-phenyl-1,3,4-thiadiazole
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H7ClN2SPurezza:Min. 95%Peso molecolare:210.68 g/mol5-(Methylsulfanyl)-1,3,4-thiadiazole-2-carbonitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H3N3S2Purezza:Min. 95%Peso molecolare:157.2 g/mol5-Phenyl-1,3,4-thiadiazole-2-carbonitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H5N3SPurezza:Min. 95%Peso molecolare:187.22 g/molN-(3-Methylbutyl)cyclopentanamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H21NPurezza:Min. 95%Peso molecolare:155.28 g/mol6-Chloropyrido[2,3-b]pyrazin-2(1H)-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H4ClN3OPurezza:Min. 95%Peso molecolare:181.58 g/molMethyl 3-hydroxy-2-methyl-2-phenylpropanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H14O3Purezza:Min. 95%Peso molecolare:194.23 g/mol1-Bromo-3-(isopropylsulfanyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11BrSPurezza:Min. 95%Peso molecolare:231.15 g/mol1-Bromo-4-(isopropylthio)benzene
CAS:<p>1-Bromo-4-(isopropylthio)benzene is a reusable, phenylboronic acid reagent. It is used in organic synthesis as a Grignard reagent or peroxide. 1-Bromo-4-(isopropylthio)benzene can be prepared by the reaction of benzene and phenylboronic acid in the presence of potassium carbonate. The reaction proceeds with high yield at room temperature and pressure. 1-Bromo-4-(isopropylthio)benzene reacts with hydrogen peroxide to form 4,5-dihydrobenzoquinone and 2-phenylethanol. This chemical is also used as an industrial acid ester and a reagent for organic synthesis.</p>Formula:C9H11BrSPurezza:Min. 95%Peso molecolare:231.15 g/mol1-Bromo-3-(isopropanesulfonyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11BrO2SPurezza:Min. 95%Peso molecolare:263.15 g/mol1-Oxa-8-azaspiro[5.5]undecane
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H17NOPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:155.24 g/mol2-(2-Methylindolizin-3-yl)ethan-1-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H14N2Purezza:Min. 95%Peso molecolare:174.24 g/mol5-(Piperidin-1-yl)pentan-1-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H22N2Purezza:Min. 95%Peso molecolare:170.3 g/mol1-Methyl-2-oxo-1,2-dihydropyridine-4-carbonitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6N2OPurezza:Min. 95%Peso molecolare:134.14 g/mol2-Acetamido-6-fluorobenzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8FNO3Purezza:Min. 95%Peso molecolare:197.16 g/molEthyl 5-oxoheptanoate
CAS:<p>Ethyl 5-oxoheptanoate is a clear, colorless liquid that can be synthesized by reacting benzene with acetone. The synthesis of ethyl 5-oxoheptanoate is an example of a Friedel-Crafts reaction. This chemical is soluble in organic solvents such as acetone and cyclohexane and has low toxicity. It can be used as a reagent for the preparation of esters from alcohols, phenols, or carboxylic acids. Ethyl 5-oxoheptanoate can also be used to prepare resorcinol, which is a precursor to polymers and dyes, by hydrogenation of the molecule. Preparative methods are often used to produce this product because it has limited solubility in water.</p>Formula:C9H16O3Purezza:Min. 95%Peso molecolare:172.22 g/mol2-Methyl-2-(phenylamino)propanamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H14N2OPurezza:Min. 95%Peso molecolare:178.23 g/mol4-(2,4-Dimethylphenoxy)butanoic acid
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C12H16O3Purezza:Min. 95%Peso molecolare:208.25 g/mol2-(Benzyloxy)-1-propanol
CAS:<p>2-(Benzyloxy)-1-propanol (2-BP) is a glycidol derivative that can be used to produce propanol. 2-BP reacts with Tenofovir, an antiviral drug, in the presence of enolate and organometallic catalysts to form acetaldehyde. 2-BP also reacts with chloride to form alkoxides, which are useful in the synthesis of adenine derivatives. In addition, 2-BP has been shown to react with vinyl ethers and alcohols in the presence of catalysis to form benzyl derivatives.</p>Formula:C10H14O2Purezza:Min. 95%Peso molecolare:166.22 g/mol3-(aminomethyl)-1-methyl-1,2-dihydropyridin-2-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10N2OPurezza:Min. 95%Peso molecolare:138.16 g/mol5-(aminomethyl)-1-methyl-2(1h)-pyridinone
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10N2OPurezza:Min. 95%Peso molecolare:138.16 g/mol1-Chloro-2-(iodomethyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6ClIPurezza:Min. 95%Peso molecolare:252.48 g/mol1-Chloro-3-(iodomethyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6ClIPurezza:Min. 95%Peso molecolare:252.48 g/mol1-(3,4-Dihydro-2H-1-benzopyran-6-yl)propan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H14O2Purezza:Min. 95%Peso molecolare:190.24 g/mol2-{[4-Phenyl-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazol-3-yl]sulfanyl}acetohydrazide
CAS:<p>Versatile small molecule scaffold</p>Formula:C19H21N5O4SPurezza:Min. 95%Peso molecolare:415.5 g/molN-[(Hydrazinecarbonyl)methyl]furan-2-carboxamide
CAS:<p>N-[(Hydrazinecarbonyl)methyl]furan-2-carboxamide is a potent and selective inhibitor of the human TRPV1 receptor. It has been used as a research tool in the study of TRPV1 function, including its role in pain perception and inflammation.</p>Formula:C7H9N3O3Purezza:Min. 95%Peso molecolare:183.16 g/mol4-(Butan-2-yloxy)phenol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H14O2Purezza:Min. 95%Peso molecolare:166.22 g/mol1-(2-Hydroxybenzoyl)pyrrolidine-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13NO4Purezza:Min. 95%Peso molecolare:235.2 g/mol7-Phenyl-pteridin-4-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H8N4OPurezza:Min. 95%Peso molecolare:224.22 g/mol1'-Methyl-3,4-dihydrospiro[1-benzopyran-2,4'-piperidine]-4-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H20N2OPurezza:Min. 95%Peso molecolare:232.32 g/mol2,4-Dimethyl-6-oxo-1-phenyl-1,6-dihydropyridine-3-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H13NO3Purezza:Min. 95%Peso molecolare:243.26 g/mol4-Bromo-3,5-dimethylpyridine 1-oxide
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8BrNOPurezza:Min. 95%Peso molecolare:202.05 g/molMethyl 3-(methoxyamino)-3-methylbutanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H15NO3Purezza:Min. 95%Peso molecolare:161.2 g/mol(2E)-3-(3,4-Dimethoxyphenyl)-2-methylprop-2-enoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H14O4Purezza:Min. 95%Peso molecolare:222.24 g/mol-3(3-Methylpyridin-2-Yl)Propanoic Acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11NO2Purezza:Min. 95%Peso molecolare:165.19 g/mol1-[4-(Pyridin-4-yl)phenyl]ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H11NOPurezza:Min. 95%Peso molecolare:197.23 g/mol5-Methylquinoline-8-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H9NO2Purezza:Min. 95%Peso molecolare:187.19 g/mol4-Methylquinoline-8-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H9NO2Purezza:Min. 95%Peso molecolare:187.19 g/mol3-Hydrazinyl-6-(1H-pyrazol-1-yl)pyridazine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8N6Purezza:Min. 95%Peso molecolare:176.18 g/mol[(3-Chloro-4-methoxyphenyl)amino]carbonitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H7ClN2OPurezza:Min. 95%Peso molecolare:182.61 g/molN,2-Dimethyl-4,5,6,7-tetrahydro-1,3-benzothiazol-7-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H14N2SPurezza:Min. 95%Peso molecolare:182.29 g/molN-Butyl-4,5,6,7-tetrahydro-1,3-benzothiazol-6-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H18N2SPurezza:Min. 95%Peso molecolare:210.34 g/mol2,4-Dichloropyridine-3-carboxamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H4Cl2N2OPurezza:Min. 95%Peso molecolare:191.02 g/mol2-(3-Methylthiophen-2-yl)acetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8O2SPurezza:Min. 95%Peso molecolare:156.2 g/mol2-Imino-4-oxo-[1,3]thiazinane-6-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H6N2O3SPurezza:Min. 95%Peso molecolare:174.18 g/molEthyl 4-oxo-3-propanoylhexanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H18O4Purezza:Min. 95%Peso molecolare:214.26 g/mol2-[3-(4-Fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C17H13FN2O2Purezza:Min. 95%Peso molecolare:296.29 g/mol2-[3-(4-Bromophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid
CAS:<p>2-[3-(4-Bromophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid is a research tool that can be used to study the interaction of peptides with ion channels, receptors and other proteins. It has been shown to inhibit the activity of various ion channels, including voltage gated sodium channels and calcium channels. 2-[3-(4-Bromophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid is also a ligand for various receptors, including opioid receptors and serotonin receptors. This chemical compound has been used in pharmacological studies as a receptor antagonist.</p>Formula:C17H13BrN2O2Purezza:Min. 95%Peso molecolare:357.2 g/mol2-[3-(4-Methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C18H16N2O3Purezza:Min. 95%Peso molecolare:308.3 g/mol2,4-Dimethylhexanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H16O2Purezza:Min. 95%Peso molecolare:144.21 g/mol2-(5-Methylthiophen-2-yl)acetic acid
CAS:<p>2-(5-Methylthiophen-2-yl)acetic acid is an organic compound that is a colorless liquid. It has been reported to be used as a bacteriostatic agent and has been found to inhibit the growth of bacteria in culture. 2-(5-Methylthiophen-2-yl)acetic acid preferentially inhibits aerobic metabolism, which may be due to its ability to inhibit the synthesis of fatty acids. This chemical also undergoes biotransformations in cultures and is readily biodegradable. Analysis of 2-(5-methylthiophen-2-yl)acetic acid can be done by gas chromatography or high performance liquid chromatography.</p>Formula:C7H8O2SPurezza:Min. 95%Peso molecolare:156.2 g/molPropylhydrazine dihydrochloride
CAS:<p>Propylhydrazine dihydrochloride is a pyrazole derivative that has been shown to have inhibitory effects on the immune system. It has been used as a treatment agent for autoimmune diseases such as rheumatoid arthritis and multiple sclerosis. Propylhydrazine dihydrochloride inhibits inflammatory responses by binding to retinoic acid receptors, blocking the production of inflammatory mediators such as prostaglandins and leukotrienes. In addition, this compound inhibits the release of histamine from mast cells, which may be due to its ability to inhibit the activity of acid receptors in these cells.</p>Formula:C3H12Cl2N2Purezza:Min. 95%Peso molecolare:147.04 g/molButylhydrazine dihydrochloride
CAS:<p>Butylhydrazine dihydrochloride is a retinoic acid analog that inhibits the production of nerve cells in the brain, thereby preventing degenerative diseases such as Alzheimer's disease. This drug has been shown to inhibit the production of nerve cells and prevent neurodegeneration in mice by targeting retinoic acid receptors. Butylhydrazine dihydrochloride is also used as a diluent for other drugs, such as pyrazolopyrimidine derivatives, which can cause death if administered alone. Butylhydrazine dihydrochloride may have an autoimmune effect, due to its ability to inhibit the production of antibodies and T-cell responses.</p>Formula:C4H14Cl2N2Purezza:Min. 95%Peso molecolare:161.07 g/molAllylhydrazine Dihydrochloride
CAS:Prodotto controllato<p>Allylhydrazine is a chemical compound that is used as an inhibitor of cellular kinases. It has been shown to inhibit the growth of colon and prostate cancer cells, as well as breast and lung cancer cells. Allylhydrazine is a disubstituted imidazole with two amino groups and one hydrazine group. This product also inhibits angiogenesis and has been shown to prevent the formation of new blood vessels in solid tumors. Allylhydrazine has been synthesized from allyl alcohol in the presence of acidified hydrogen chloride gas, providing a yield of about 50%.</p>Formula:C3H10Cl2N2Purezza:Min. 95%Peso molecolare:145.03 g/mol4-(3-Fluorophenyl)butanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11FO2Purezza:Min. 95%Peso molecolare:182.19 g/mol4-(4-Methoxyphenyl)-6-oxo-2-sulfanyl-1,6-dihydropyrimidine-5-carbonitrile
CAS:<p>4-(4-Methoxyphenyl)-6-oxo-2-sulfanyl-1,6-dihydropyrimidine-5-carbonitrile (DMP) is a potentiodynamic polarization and electrochemical impedance spectroscopic technique that can be used to measure the corrosion inhibition efficiency of anodic inhibitors. DMP is an electron donor that can reduce the concentration of chloride ions and copper ions on the anode surface. It also has a strong inhibition effect on both kinetic and equilibrium corrosion reactions. The impedance analysis of DMP shows that it does not have any significant effect on the elements in the solution, such as copper, chloride, or sulfuric acid. This suggests that DMP is a good inhibitor for corrosion reactions in alkaline solutions.</p>Formula:C12H9N3O2SPurezza:Min. 95%Peso molecolare:259.29 g/mol2-oxo-1,2-dihydroquinoline-6-carboxylic acid
CAS:<p>Quinoline-2-carboxylic acid is a quinoline residue that has been hydrolyzed to the corresponding 2-oxo-1,2-dihydroquinoline-6-carboxylic acid. It is an alkoxy, alkenyl, and cardiotonic drug that has been used as a carbostyril skeleton.</p>Formula:C10H7NO3Purezza:Min. 95%Peso molecolare:189.17 g/mol3-Nitro-4-phenyl-1H-pyrrole
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H8N2O2Purezza:Min. 95%Peso molecolare:188.18 g/mol1-Bromo-2-(chloromethyl)cyclopropane
CAS:<p>1-Bromo-2-(chloromethyl)cyclopropane is a methylenecyclopropane that reacts with thiophenol to form an anion. This reaction can be catalyzed by bases or acid. 1-Bromo-2-(chloromethyl)cyclopropane reacts with alcohols to produce nitriles, which are compounds containing the functional group, -C(O)NRR'. Nitriles can also be formed by the direct reaction of anions and alcohols, but this process is less efficient. 1-Bromo-2-(chloromethyl)cyclopropane is used as a solvent in organic chemistry because it reacts with many substances and forms new compounds.</p>Formula:C4H6BrClPurezza:Min. 95%Peso molecolare:169.4 g/mol4-Bromo-2,6-dimethoxyphenol
CAS:<p>4-Bromo-2,6-dimethoxyphenol is a synthetic intramolecular nucleophilic substitution product of 2,6-dimethoxybenzaldehyde. The asymmetric synthesis of 4-bromo-2,6-dimethoxyphenol was achieved by the biomimetic strategy. This reaction is catalyzed by palladium and utilizes a chiral phosphine ligand.</p>Formula:C8H9BrO3Purezza:Min. 95%Peso molecolare:233.06 g/mol2-Methoxyquinoline-3-carboxylic acid
CAS:<p>2-Methoxyquinoline-3-carboxylic acid is an alkaloid that was synthesized by the methoxylation of 2-methoxyquinoline. This compound has been shown to be a good analogue for optimising the reaction between acetone and bromine in order to produce dehydrobrominated compounds. The redox reaction of this compound with hydrogen peroxide is also interesting, as it produces hydrogen gas in addition to the desired products.</p>Formula:C11H9NO3Purezza:Min. 95%Peso molecolare:203.19 g/mol2-(Methylamino)pyridine-3-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H9N3O2SPurezza:Min. 95%Peso molecolare:187.22 g/mol(2S)-2-Bromo-3-hydroxypropanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C3H5BrO3Purezza:Min. 95%Peso molecolare:168.97 g/mol5-Bromo-3-methylbenzo[D]oxazol-2(3H)-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H6BrNO2Purezza:Min. 95%Peso molecolare:228.04 g/mol
