Building Blocks
This section contains fundamental products for the synthesis of organic and biological compounds. Building blocks are the essential starting materials used to construct complex molecules through various chemical reactions. They play a critical role in drug discovery, material science, and chemical research. At CymitQuimica, we offer a diverse range of high-quality building blocks to support your innovative research and industrial projects, ensuring you have the essential components for successful synthesis.
Subcategories of "Building Blocks"
- Boronic Acids & Boronic Acid Derivatives(5,781 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,101 products)
- Organic Building Blocks(61,038 products)
Found 205338 products of "Building Blocks"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
1-tert-Butyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C10H13NO3Purity:Min. 95%Molecular weight:195.21 g/mol3-Methylisatoic anhydride
CAS:Versatile small molecule scaffoldFormula:C9H7NO3Purity:Min. 95%Molecular weight:177.16 g/mol5-(3-Methylphenoxymethyl)-1,3,4-oxadiazole-2-thiol
CAS:Versatile small molecule scaffoldFormula:C10H10N2O2SPurity:Min. 95%Molecular weight:222.27 g/mol5-(Pyrrolidin-1-yl)-1,3,4-thiadiazole-2-thiol
CAS:Versatile small molecule scaffoldFormula:C6H9N3S2Purity:Min. 95%Molecular weight:187.3 g/mol5-(Piperidin-1-yl)-1,3,4-thiadiazole-2-thiol
CAS:Versatile small molecule scaffoldFormula:C7H11N3S2Purity:Min. 95%Molecular weight:201.3 g/mol5-[(2-Methylpropyl)amino]-1,3,4-thiadiazole-2-thiol
CAS:5-[(2-Methylpropyl)amino]-1,3,4-thiadiazole-2-thiol is a modification of the oligosaccharide. It is a monosaccharide with a methyl group at the C5 position and a fluorine atom at the C4 position. 5-[(2-Methylpropyl)amino]-1,3,4-thiadiazole-2-thiol is synthesized by reacting 2-(methylpropyl)amine with thiadiazole dithiole. This compound has CAS No. 66180-54-9 and can be used as an intermediate in the synthesis of complex carbohydrates. The carbohydrate structure of 5-[(2-Methylpropyl)amino]-1,3,4-thiadiazole-2-thiol consists of a glycosidic linkage between two saccharides: a hexose and an acetalFormula:C6H11N3S2Purity:Min. 95%Molecular weight:189.3 g/mol7-Methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-3-one
CAS:Versatile small molecule scaffoldFormula:C11H13NO2Purity:Min. 95%Molecular weight:191.23 g/mol2-[(2-Bromophenyl)methyl]butanoic acid
CAS:Versatile small molecule scaffoldFormula:C11H13BrO2Purity:Min. 95%Molecular weight:257.12 g/mol3-(2-Bromo-5-methoxyphenyl)propanoic acid
CAS:Versatile small molecule scaffoldFormula:C10H11BrO3Purity:Min. 95%Molecular weight:259.1 g/mol3-(2-Bromo-4-chlorophenyl)propanoic acid
CAS:Versatile small molecule scaffold
Formula:C9H8BrClO2Purity:Min. 95%Molecular weight:263.51 g/mol3-(2-bromo-5-chlorophenyl)propanoic acid
CAS:Versatile small molecule scaffold
Formula:C9H8BrClO2Purity:Min. 95%Molecular weight:263.5 g/mol2-Bromo-4-chloro-1-(chloromethyl)benzene
CAS:Versatile small molecule scaffold
Formula:C7H5BrCl2Purity:Min. 95%Molecular weight:239.92 g/molMethyl 5,6,7,8-tetrahydronaphthalene-1-carboxylate
CAS:Versatile small molecule scaffoldFormula:C12H14O2Purity:Min. 95%Molecular weight:190.24 g/mol3-Benzylpyrrolidine-2,5-dione
CAS:3-Benzylpyrrolidine-2,5-dione is a potent and selective serine protease inhibitor. It binds to the active site of the enzyme, blocking the formation of an acyl enzyme intermediate that is required for biological activity. 3-Benzylpyrrolidine-2,5-dione is effective at inhibiting a wide range of serine proteases, including those from bacteria and viruses. This drug has been shown to be chemically stable in solution and does not react with other molecules in solution, which may be due to its carbonyl group. 3-Benzylpyrrolidine-2,5-dione also irreversibly inhibits serine proteases by covalent modification of key amino acid residues on the enzyme's active site.Formula:C11H11NO2Purity:Min. 95%Molecular weight:189.21 g/mol2-Iodo-6-methoxybenzoic acid
CAS:Versatile small molecule scaffold
Formula:C8H7IO3Purity:Min. 95%Molecular weight:278.04 g/molDiethyl bromomethylphosphonate
CAS:Diethyl bromomethylphosphonate is a chemical compound with fatty acid properties. It is used as an inhibitor in pharmaceutical preparations and has been shown to be bactericidal to animals. Diethyl bromomethylphosphonate also inhibits the enzyme fatty acid synthase, which catalyzes the formation of fatty acids from acetyl-CoA and malonyl-CoA. This inhibitor is used in the treatment of congestive heart failure and insulin resistance. Diethyl bromomethylphosphonate is a functional group that can undergo hydrolysis by hydrochloric acid, leading to the release of diethyl methylphosphonite. Diethyl bromomethylphosphonate is a chemical compound that can react with organic solvents such as water or alcohols for reactions.Formula:C5H12BrO3PPurity:Min. 95%Molecular weight:231.03 g/mol3-Chlorofuran-2-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C5H3ClO3Purity:Min. 95%Molecular weight:146.53 g/molEthyl 1,3-thiazolidine-4-carboxylate hydrochloride
CAS:Versatile small molecule scaffold
Formula:C6H12ClNO2SPurity:Min. 95%Molecular weight:197.68 g/mol2-Acetamido-6-methylbenzoic acid
CAS:Versatile small molecule scaffoldFormula:C10H11NO3Purity:Min. 95%Molecular weight:193.2 g/mol7-(Aminomethyl)-5-chloroquinolin-8-ol dihydrochloride
CAS:Versatile small molecule scaffoldFormula:C10H11Cl3N2OPurity:Min. 95%Molecular weight:281.6 g/mol
![5-[(2-Methylpropyl)amino]-1,3,4-thiadiazole-2-thiol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRCA18054.webp&w=3840&q=75)
![2-[(2-Bromophenyl)methyl]butanoic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRCA19200.webp&w=3840&q=75)
