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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3-(Chloromethyl)-5H,6H,8H-[1,2,4]triazolo[3,4-c][1,4]oxazine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H9Cl2N3OPurity:Min. 95%Molecular weight:210.06 g/molRef: 3D-DXC56271
Discontinued product(2S,3R,4S,5S,6R)-2-(1,3-Dioxaindan-4-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H16O8Purity:Min. 95%Molecular weight:300.26 g/molRef: 3D-FDD47456
Discontinued product3-Amino-1,1-diethoxypropan-2-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H17NO3Purity:Min. 95%Molecular weight:163.21 g/molRef: 3D-QEA82718
Discontinued product4-(Cyclopropylmethoxy)-2-fluoroaniline hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H13ClFNOPurity:Min. 95%Molecular weight:217.67 g/molMethyl 4-methyl-3-{[(4-methyl-1H-imidazol-5-yl)methyl]amino}benzoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H17N3O2Purity:Min. 95%Molecular weight:259.3 g/molRef: 3D-QCC36887
Discontinued productEthyl 3-(5-bromo-2-methoxyphenyl)-3-hydroxypropanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H15BrO4Purity:Min. 95%Molecular weight:303.15 g/molRef: 3D-QCC36863
Discontinued producttert-butyl (2S)-2-aminohexanoate
CAS:<p>Tert-butyl (2S)-2-aminohexanoate is an intermediate that is used in the synthesis of glycine by the reaction of benzyl bromide and tert-butyl amine. The stereospecifically incorporated tert-butyl group has a high degree of enantioselectivity, which makes this intermediate useful in the synthesis of glycine. Tert-butyl (2S)-2-aminohexanoate can be synthesized using lithium diisopropylamide and a tertiary amine as an alkylating agent.</p>Formula:C10H21NO2Purity:Min. 95%Molecular weight:187.3 g/mol2-(2,4-Dimethylbenzoyl)furan
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H12O2Purity:Min. 95%Molecular weight:200.23 g/mol4-Methanesulfonyl-N-methoxy-N-methylbenzamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H13NO4SPurity:Min. 95%Molecular weight:243.28 g/molRef: 3D-FDC90510
Discontinued product1-(2-Bromoethoxy)-2-nitrobenzene
CAS:<p>1-(2-Bromoethoxy)-2-nitrobenzene is a fluorescent ionophore that is used in the production of high-performance liquid chromatography (HPLC) columns. This chemical is synthesized by a stepwise reaction that starts with the formation of an acetonitrile adduct. The acetonitrile group is then removed and replaced with an ethoxy group to form the final product. The synthetic procedure for 1-(2-bromoethoxy)-2-nitrobenzene has been rationalized and it can be recycled using magnesium as a reducing agent. In addition, this chemical has been shown to bind to sensor proteins due to its high affinity for them.</p>Formula:C8H8BrNO3Purity:Min. 95%Molecular weight:246.06 g/mol2-(N-Boc-amino)-5-(tributylstannyl)thiazole
CAS:Controlled Product<p>Versatile small molecule scaffold</p>Formula:C20H38N2O2SSnPurity:Min. 95%Molecular weight:489.3 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/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
![3-(Chloromethyl)-5H,6H,8H-[1,2,4]triazolo[3,4-c][1,4]oxazine hydrochloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FDXC56271.webp&w=3840&q=75)
![Methyl 4-methyl-3-{[(4-methyl-1H-imidazol-5-yl)methyl]amino}benzoate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FQCC36887.webp&w=3840&q=75)
![3-Boc-3-azabicyclo[3.2.1]octan-8-amine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFDC76351.webp&w=3840&q=75)
