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(61,055 products)
Found 199650 products of "Building Blocks"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
4-(Chloromethyl)-1,4-dimethylpiperidine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H17Cl2NPurity:Min. 95%Molecular weight:198.13 g/molRef: 3D-DXC58362
Discontinued productMethyl 2-[4-(2-aminoethyl)phenoxy]acetate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H16ClNO3Purity:Min. 95%Molecular weight:245.7 g/mol2-(2,4-Difluorophenyl)propanedinitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H4F2N2Purity:Min. 95%Molecular weight:178.14 g/molRef: 3D-DXC58290
Discontinued product2-(Aminomethyl)-N-tert-butylbenzene-1-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H18N2O2SPurity:Min. 95%Molecular weight:242.34 g/mol3-[(2-Methyl-2-propen-1-yl)thio]-5H-1,2,4-triazino[5,6-b]indole
CAS:<p>3-[(2-Methyl-2-propen-1-yl)thio]-5H-1,2,4-triazino[5,6-b]indole is a recombinant protein that binds to the ribosomal protein L11. It has been shown to inhibit the biosynthesis of the bacterial cell wall and therefore inhibit replication of the bacterial genome. 3-[(2-Methyl-2-propen-1-yl)thio]-5H-1,2,4-triazino[5,6-b]indole also inhibits the synthesis of proteins essential for cell division. This compound has been shown to bind to ribosomes in both prokaryotic and eukaryotic cells. It may have potential as an inhibitor of cancerous cells because it inhibits protein synthesis in mammalian cells.</p>Formula:C13H12N4SPurity:Min. 95%Molecular weight:256.33 g/molRef: 3D-DNA02311
Discontinued product4-[1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]aniline
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H10F3N3Purity:Min. 95%Molecular weight:241.21 g/molRef: 3D-GHC38675
Discontinued productrac-(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 product4-Chloro-N,N-diethyl-butyramide
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H16ClNOPurity:Min. 95%Molecular weight:177.67 g/molRef: 3D-GCA79428
Discontinued product3-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/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/mol
