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(6,093 products)
- Organic Building Blocks(60,525 products)
Found 195533 products of "Building Blocks"
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2-Bromo-5-ethynylpyridine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H4BrNPurity:Min. 95%Molecular weight:182.02 g/molRef: 3D-UXA67228
Discontinued product1-(2-Methylpyrimidin-4-yl)ethan-1-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H11N3Purity:Min. 95%Molecular weight:137.18 g/molRef: 3D-JJC20141
Discontinued producttert-Butyl N-{2-amino-1-[4-(propan-2-yl)phenyl]ethyl}carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C16H26N2O2Purity:Min. 95%Molecular weight:278.39 g/mol2-Isocyanato-1-methoxybutane
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H11NO2Purity:Min. 95%Molecular weight:129.2 g/molRef: 3D-MBA44101
Discontinued productMethyl-2-benzyl-5-methyl-octahydro-1H-pyrrolo[3,4-c]pyridine-7a-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C17H24N2O2Purity:Min. 95%Molecular weight:288.4 g/mol2-(Oxan-4-yl)butanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H16O3Purity:Min. 95%Molecular weight:172.22 g/molRef: 3D-VXB34063
Discontinued product4-Chloro-3,3-dimethylbutan-2-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H11ClOPurity:Min. 95%Molecular weight:134.6 g/molRef: 3D-NAA10453
Discontinued productNaphthalene-2-carboximidamide
CAS:<p>Naphthalene-2-carboximidamide is a benzamidine derivative that interacts with the active site of serine proteases. It was shown to have potent inhibitory potency against a number of proteinases, including urokinase-type plasminogen activator (uPA), matrix metalloproteinase-9 (MMP-9), and cathepsin G. The interaction of naphthalene-2-carboximidamide with uPA was specific and led to inhibition of its catalytic activity. Naphthalene-2-carboximidamide has been tested in clinical trials for the treatment of influenza.</p>Formula:C11H10N2Purity:Min. 95%Molecular weight:170.21 g/mol[2-(Piperidin-1-yl)pyridin-3-yl]methanamine dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H19Cl2N3Purity:Min. 95%Molecular weight:264.19 g/molRef: 3D-FDD50657
Discontinued product(1-Bromocyclopentyl)(phenyl)methanone
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13BrOPurity:Min. 95%Molecular weight:253.13 g/molRef: 3D-GAA74066
Discontinued product5-(Iodomethyl)-2-phenyl-4,5-dihydro-1,3-oxazole
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10INOPurity:Min. 95%Molecular weight:287.1 g/molRef: 3D-AIA57305
Discontinued product2-Cyano-5-fluorophenol
CAS:<p>2-Cyano-5-fluorophenol is an organic compound that is used as a precursor to medicines and other chemicals. It reacts with calcium hydroxide in water to form 2-cyano-5-hydroxyfluorobenzene, which can be hydrolyzed to form 2-cyano-5-chlorofluorobenzene. This compound can also react with sodium hydroxide to produce sodium cyanate, which can be hydrolyzed to form sodium chloride and hydrogen cyanide gas. The alkali metal ions are needed for this reaction, which is why the product should not be exposed to water or moisture. 2-Cyano-5-fluorophenol has been shown to have liquid crystal properties and is used in the production of certain types of polymers. 2Cyano-5Fluorophenol crystals are also used in some medicines such as acetaminophen (paracetamol).</p>Formula:C7H4FNOPurity:Min. 95%Molecular weight:137.11 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
![tert-Butyl N-{2-amino-1-[4-(propan-2-yl)phenyl]ethyl}carbamate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FUQB35517.webp&w=3840&q=75)
![Methyl-2-benzyl-5-methyl-octahydro-1H-pyrrolo[3,4-c]pyridine-7a-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FVXC57025.webp&w=3840&q=75)
![[2-(Piperidin-1-yl)pyridin-3-yl]methanamine dihydrochloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFDD50657.webp&w=3840&q=75)
