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"
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rac-(1R,5S,6R)-3-Benzyl-3-azabicyclo[3.1.0]hexan-6-amine dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H18Cl2N2Purity:Min. 95%Molecular weight:261.19 g/molRef: 3D-DJD39547
Discontinued product7-Hydroxy-3,4-dimethyl-2,3-dihydro-1H-inden-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H12O2Purity:Min. 95%Molecular weight:176.21 g/mol2-(2-Bromo-ethoxy)-1,4-dimethyl-benzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H13BrOPurity:Min. 95%Molecular weight:229.12 g/mol2-Amino-4H,5H-naphtho[2,1-b]thiophene-1-carbonitrile
CAS:<p>2-Amino-4H,5H-naphtho[2,1-b]thiophene-1-carbonitrile is a dihydronaphthalene compound that has been shown to be active against influenza viruses. It inhibits the virus by binding to the pyrimidine ring of the virus's RNA polymerase. This inhibits viral replication and reduces plaque formation. 2-Amino-4H,5H-naphtho[2,1-b]thiophene-1-carbonitrile has antiviral activity against influenza A and is effective in inhibiting h5n1 virus replication.</p>Formula:C13H10N2SPurity:Min. 95%Molecular weight:226.3 g/mol3-(1-Benzyl-1H-1,2,3-triazol-4-yl)aniline
CAS:<p>Versatile small molecule scaffold</p>Formula:C15H14N4Purity:Min. 95%Molecular weight:250.3 g/molRef: 3D-BWB92000
Discontinued product3-Amino-4,4-dimethylpentan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H17NOPurity:Min. 95%Molecular weight:131.22 g/mol1-(1-Methyl-1H-indazol-5-yl)ethanone
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10N2OPurity:Min. 95%Molecular weight:174.2 g/mol1-(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 producttert-butyl 3-(aminomethyl)azepane-1-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H24N2O2Purity:Min. 95%Molecular weight:228.3 g/molRef: 3D-BKB14747
Discontinued productQuinoline-5-carbonitrile
CAS:<p>Quinoline-5-carbonitrile is a cyanide compound that can be used in the synthesis of heterocyclic compounds. The reaction between quinoline and 5-cyanovaleric acid produces 6-nitroquinoline, which is then converted to dimethyl sulfoxide by alcoholysis. This reaction product can then be used to synthesize an amide or nucleophile. Quinoline-5-carbonitrile reacts with potassium in the presence of bifunctional hydrazide to produce a cyanide ion, which can be hydrolyzed by an acid to release hydrogen cyanide gas. This experiment has been shown as a model for reactions involving cyano compounds.</p>Formula:C10H6N2Purity:Min. 95%Molecular weight:154.17 g/molRef: 3D-JCA55102
Discontinued productN-(5-Bromo-2-methylpyridin-3-yl)acetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9BrN2OPurity:Min. 95%Molecular weight:229.07 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
