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(5,756 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,095 products)
- Organic Building Blocks(61,051 products)
Found 199813 products of "Building Blocks"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
2-Methyl-3-(1,3-oxazol-2-yl)aniline dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H12Cl2N2OPurity:Min. 95%Molecular weight:247.12 g/molRef: 3D-JBD31004
Discontinued product2-(2-Methyl-2,3-dihydro-1-benzofuran-5-yl)ethan-1-amine
CAS:Controlled Product<p>Versatile small molecule scaffold</p>Formula:C11H15NOPurity:Min. 95%Molecular weight:177.24 g/molMethyl 1-amino-3-methylcyclobutane-1-carboxylate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H14ClNO2Purity:Min. 95%Molecular weight:179.6 g/molRef: 3D-UTD67810
Discontinued productMethyl 2-amino-3,3-dimethylbutanoate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H16ClNO2Purity:Min. 95%Molecular weight:181.66 g/molN-Methyl-4-phenoxyaniline
CAS:<p>N-Methyl-4-phenoxyaniline is a molecule that inhibits chitinase, an enzyme that catalyzes the hydrolysis of chitin, and molting. N-Methyl-4-phenoxyaniline has been shown to be potent inhibitor of the enzyme amide in vitro. It also inhibits onchocerca volvulus and in vivo, which may be due to its ability to inhibit the synthesis of fatty acids. This drug has not been tested against other parasites or mammals, but it is an anthelmintic drug.</p>Formula:C13H13NOPurity:Min. 95%Molecular weight:199.25 g/molN-Cyclopropyl-N-methylaminosulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H10N2O2SPurity:Min. 95%Molecular weight:150.2 g/molRef: 3D-XPA13681
Discontinued product1-(1-Benzothiophen-2-yl)-2-methoxyethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H10O2SPurity:Min. 95%Molecular weight:206.3 g/molRef: 3D-BPC71122
Discontinued product3-Amino-4,4-dimethylpentan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H17NOPurity:Min. 95%Molecular weight:131.22 g/mol4-Methyl-1H-indazol-7-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9N3Purity:Min. 95%Molecular weight:147.18 g/mol1-(Butan-2-yl)-5-cyclopropyl-1H-pyrazol-4-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H17N3Purity:Min. 95%Molecular weight:179.26 g/molRef: 3D-GQB45453
Discontinued product8-Methoxy-2,3,4,5-tetrahydro-1,4-benzoxazepin-5-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11NO3Purity:Min. 95%Molecular weight:193.2 g/mol2-Bromo-3,3,3-trifluoro-1-propene
CAS:Controlled Product<p>2-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%.</p>Formula:C3H2BrF3Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:174.95 g/mol3-Boc-3-azabicyclo[3.2.1]octan-8-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H22N2O2Purity:Min. 95%Molecular weight:226.32 g/mol
