Building Blocks
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.778 prodotti)
- Building Blocks Chirali(1.243 prodotti)
- Building Blocks Idrocarburici(6.098 prodotti)
- Building Blocks organici(61.042 prodotti)
Trovati 204339 prodotti di "Building Blocks"
(3-bromo-5-iodophenyl)methanol
CAS:Versatile small molecule scaffold
Formula:C7H6BrIOPurezza:Min. 95%Peso molecolare:312.9 g/mol2-[(4-Aminophenyl)sulfanyl]-5-chlorobenzonitrile
CAS:Versatile small molecule scaffold
Formula:C13H9ClN2SPurezza:Min. 95%Peso molecolare:260.74 g/mol2-Methyl-2-(pyrrolidin-1-yl)propanoic acid hydrochloride
CAS:Versatile small molecule scaffold
Formula:C8H16ClNO2Purezza:Min. 95%Peso molecolare:193.67 g/mol4-(1-Aminoethyl)-N-methylbenzene-1-sulfonamide
CAS:Versatile small molecule scaffold
Formula:C9H14N2O2SPurezza:Min. 95%Peso molecolare:214.29 g/mol5-Methyl-1,4-thiazepane-1,1-dione hydrochloride
CAS:Versatile small molecule scaffold
Formula:C6H14ClNO2SPurezza:Min. 95%Peso molecolare:199.7 g/mol1-(Butane-1-sulfonyl)piperidine-2-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C10H19NO4SPurezza:Min. 95%Peso molecolare:249.33 g/mol2-[1-(Difluoromethyl)-3,5-dimethyl-1H-pyrazol-4-yl]acetic acid
CAS:Prodotto controllato2-[1-(Difluoromethyl)-3,5-dimethyl-1H-pyrazol-4-yl]acetic acid is a potent inhibitor of peptide binding to the receptor. It has a Kd value of 0.2 μM and a Ki value of 1.6 μM in the inhibition of insulin binding to its receptor. 2-[1-(Difluoromethyl)-3,5-dimethyl-1H-pyrazol-4-yl]acetic acid is also an activator of protein interactions and ligand for research tools used for studying ion channels and other receptors. This chemical can be used as high purity reagent for life sciences, including cell biology and pharmacology.
Formula:C8H10F2N2O2Purezza:Min. 95%Peso molecolare:204.17 g/mol(2-Chloro-1-methyl-1H-imidazol-5-yl)methanol
CAS:Versatile small molecule scaffoldFormula:C5H7ClN2OPurezza:Min. 95%Peso molecolare:146.57 g/mol5-[(2,4-Difluorophenyl)methyl]-4-methyl-1,3-thiazol-2-amine hydrobromide
CAS:Versatile small molecule scaffold
Formula:C11H11BrF2N2SPurezza:Min. 95%Peso molecolare:321.19 g/mol3,6-Dimethyl-1-{[(propan-2-yl)carbamoyl]methyl}-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C14H18N4O3Purezza:Min. 95%Peso molecolare:290.32 g/molrac-(1R,3R)-3-Ethoxycyclobutan-1-amine hydrochloride
CAS:Versatile small molecule scaffoldFormula:C6H14ClNOPurezza:Min. 95%Peso molecolare:151.63 g/molPB-22 3-carboxyindole metabolite solution
CAS:Prodotto controllatoPB-22 is a synthetic cannabinoid, which can be classified as a CB1 receptor agonist. It is one of the many cannabinoids that have been created in an attempt to circumvent drug laws by creating compounds that are similar to those found in cannabis but have different chemical structures. PB-22 has shown to increase locomotor activity and stimulate the cb1 receptor in mice. Magnetic resonance spectroscopy (MRS) and assays were used to determine the binding affinity of PB-22 for the CB1 receptor. The MRS data showed that PB-22 bound with high affinity to the CB1 receptor and had a lower affinity for CB2 receptors. This suggests that PB-22 may be more potent than other synthetic cannabinoids, such as JWH-018 and CP 55,940, which bind better with CB2 receptors than CB1 receptors.
PB-22 is an analog of JWH-073 and has been shown to have a stronger effect on locomotor activity than JWHFormula:C14H17NO2Purezza:Min. 95%Peso molecolare:231.29 g/mol[3-Bromo-4-(morpholin-4-yl)phenyl]methanol
CAS:Versatile small molecule scaffold
Formula:C11H14BrNO2Purezza:Min. 95%Peso molecolare:272.14 g/mol4-Amino-3-phenylbutan-1-ol
CAS:Versatile small molecule scaffold
Formula:C10H15NOPurezza:Min. 95%Peso molecolare:165.23 g/mol1,1-Dioxo-2,3-dihydro-1,2-benzothiazol-6-amine
CAS:Versatile small molecule scaffold
Formula:C7H8N2O2SPurezza:Min. 95%Peso molecolare:184.22 g/mol2-Allylcyclohexanone
CAS:2-Allylcyclohexanone is an unsaturated ketone that is synthesized by the ring-opening of allyl cyclohexane carboxylate with sodium hydroxide. It can be used as a chemical intermediate for the synthesis of other compounds. 2-Allylcyclohexanone can also be used to react with hydroxide solution to produce a salt and an alcohol. The hydroxide solution can act as a base, reducing the carbonyl group in the presence of an acid to form the corresponding alcohol. This reaction is stereoselective because it only occurs when there are two different groups on adjacent carbons.
2-Allylcyclohexanone has been shown to inhibit non-nucleoside reverse transcriptase inhibitors (NNRTIs) such as nevirapine, efavirenz, and delavirdine. In addition, it has been found to have functional groups that are capable of reactingFormula:C9H14OPurezza:Min. 95%Peso molecolare:138.21 g/mol2-Amino-3-Bromo-6-trifluoromethylpyridine
CAS:Versatile small molecule scaffoldFormula:C6H4BrF3N2Purezza:Min. 95%Peso molecolare:241.01 g/mol4-Bromo-1-N-cyclopropylbenzene-1,2-diamine
CAS:Versatile small molecule scaffoldFormula:C9H11BrN2Purezza:Min. 95%Peso molecolare:227.1 g/mol[1-(Fluoromethyl)cyclopropyl]methanesulfonyl chloride
CAS:Versatile small molecule scaffold
Formula:C5H8ClFO2SPurezza:Min. 95%Peso molecolare:186.63 g/mol2-(2-Chlorophenyl)cyclohexan-1-one
CAS:Versatile small molecule scaffold
Formula:C12H13ClOPurezza:Min. 95%Peso molecolare:208.68 g/mol(1S)-1-(Oxan-4-yl)ethan-1-ol
CAS:Versatile small molecule scaffold
Formula:C7H14O2Purezza:Min. 95%Peso molecolare:130.18 g/mol3-(3-Fluoro-4-methoxyphenyl)pyridine
CAS:Versatile small molecule scaffold
Formula:C12H10FNOPurezza:Min. 95%Peso molecolare:203.21 g/mol5-Bromo-2,7-dimethyl-1H-1,3-benzodiazole
CAS:Versatile small molecule scaffoldFormula:C9H9BrN2Purezza:Min. 95%Peso molecolare:225.08 g/mol2-(6,7-Difluoro-1-benzofuran-3-yl)acetic acid
CAS:Versatile small molecule scaffold
Formula:C10H6F2O3Purezza:Min. 95%Peso molecolare:212.15 g/mol(3S)-3-Amino-3-(4-phenylphenyl)propan-1-ol hydrochloride
CAS:Versatile small molecule scaffoldFormula:C15H18ClNOPurezza:Min. 95%Peso molecolare:263.8 g/molPyrrolo[1,2-b]pyridazin-4(1H)-one
CAS:Versatile small molecule scaffold
Formula:C7H6N2OPurezza:Min. 95%Peso molecolare:134.14 g/molrac-(1R,2R)-2-(Benzyloxy)cyclohexan-1-ol
CAS:Versatile small molecule scaffold
Formula:C13H18O2Purezza:Min. 95%Peso molecolare:206.28 g/mol4-(Perfluoroethoxy)aniline
CAS:Versatile small molecule scaffold
Formula:C8H6F5NOPurezza:Min. 95%Peso molecolare:227.13 g/mol1,2,3,4,5-Pentachlorobenzene
CAS:1,2,3,4,5-Pentachlorobenzene is a chlorinated hydrocarbon that is used in the production of pesticides and herbicides. It is an ingredient in the manufacturing of pentachlorophenol and pentachloronitrobenzene. 1,2,3,4,5-Pentachlorobenzene has been used as a chemical intermediate or solvent for the production of other chemicals. The emissions from this chemical can be harmful to humans and animals because it has been shown to affect enzyme activities at sublethal doses. It also affects rat liver microsomes and causes DNA damage that can lead to cancer.
Formula:C6HCl5Purezza:Min. 95%Peso molecolare:250.34 g/mol2,2-Dibromopropane
CAS:2,2-Dibromopropane is a synthetic chemical that has been used as a precursor in the production of nylon. It is an activator that can be used to form covalent bonds with reactive groups on other molecules. The activation energy for the reaction with piperazine is between 104 and 106 kJ/mol. 2,2-Dibromopropane undergoes acylation reactions under certain conditions, forming reaction products such as 2,2-dibromoethyl acetate and 2,2-dibromoethanol. The molecular weight of 2,2-dibromopropane is 192.19 g/mol and its structural formula is CHBrCHBrCHBrCHBrC≡C≡C≡C≡C≡C≡CC(O)OH.
Formula:C3H6Br2Purezza:Min. 95%Peso molecolare:201.89 g/mol1-Monotetranoin
CAS:1-Monotetranoin is a fatty ester that is involved in the process of lipolysis, which is the breakdown of fat cells. Lipolysis occurs when an enzyme called lipase hydrolyzes triglycerides into glycerol and three fatty acids. 1-Monotetranoin has been shown to be a potent stimulator of growth factor production and cell proliferation in vivo models. It has also been shown to be effective at inhibiting angiogenic processes in vitro, including the release of growth factors from fat cells. The neutral pH optimum for 1-monotetranoin is between 7 and 8, which may be due to its hydrophobic nature.
Formula:C7H14O4Purezza:Min. 95%Peso molecolare:162.18 g/mol3-(Aminomethyl)-2,2-difluoropentane hydrochloride
CAS:Versatile small molecule scaffoldFormula:C6H14ClF2NPurezza:Min. 95%Peso molecolare:173.6 g/mol1-Boc-piperidine-2-boronic Acid Pinacol Ester
CAS:Versatile small molecule scaffoldFormula:C16H30BNO4Purezza:Min. 95%Peso molecolare:311.23 g/mol2-Chloro-1-(1-methyl-1H-imidazol-2-yl)ethan-1-one
CAS:Versatile small molecule scaffold
Formula:C6H7ClN2OPurezza:Min. 95%Peso molecolare:158.58 g/mol5-(4-Fluorophenoxymethyl)-1,3,4-oxadiazole-2-thiol
CAS:Versatile small molecule scaffoldFormula:C9H7FN2O2SPurezza:Min. 95%Peso molecolare:226.23 g/mol(6-Methylpyridin-3-yl)thiourea
CAS:Versatile small molecule scaffold
Formula:C7H9N3SPurezza:Min. 95%Peso molecolare:167.23 g/molN-tert-Butyl-2-sulfanylacetamide
CAS:Versatile small molecule scaffold
Formula:C6H13NOSPurezza:Min. 95%Peso molecolare:147.2 g/mol2-Bromo-3,3,3-trifluoro-1-propene
CAS:Prodotto controllato2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.
Formula:C3H2BrF3Purezza:Min. 95%Colore e forma:Colorless PowderPeso molecolare:174.95 g/molPiperyline
CAS:Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.
Formula:C16H17NO3Purezza:Min. 95%Peso molecolare:271.31 g/mol
