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(5,778 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,098 products)
- Organic Building Blocks(61,059 products)
Found 199580 products of "Building Blocks"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
2-[(4-Methanesulfonylphenyl)sulfanyl]benzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H12O4S2Purity:Min. 95%Molecular weight:308.4 g/mol1-(2-Chloroethanesulfonyl)-3-methoxybenzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11ClO3SPurity:Min. 95%Molecular weight:234.7 g/mol1-Chloro-4-[(2-chloroethyl)sulfonyl]benzene
CAS:Versatile small molecule scaffoldFormula:C8H8Cl2O2SPurity:Min. 95%Molecular weight:239.12 g/molrac-(1S,3S)-3-Phenylcyclobutane-1-carboxylic acid
CAS:<p>Rac-1-phenylcyclobutane-1-carboxylic acid is a carbanion that contains a cyclopropylcarbinyl group. It can be prepared by the reaction of ketones with lithium diisopropylamide. Rac-1-phenylcyclobutane-1-carboxylic acid is used as an intermediate in the synthesis of drugs such as ampicillin and erythromycin.</p>Formula:C11H12O2Purity:Min. 95%Molecular weight:176.21 g/mol7-Methylpyrazolo[1,5-a]pyridine-3-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8N2O2Purity:Min. 95%Molecular weight:176.17 g/mol3-Oxo-1-cyclohexanecarboxylic acid
CAS:<p>3-Oxo-1-cyclohexanecarboxylic acid is a structural isomer of cyclohexanecarboxylic acid. It is a white crystalline solid that can react with monoxide to form 3-oxocyclohexane carboxylic acid or with chlorine to form 3-chlorocyclohexane carboxylic acid. The reaction rate and regioselectivity are dependent on the catalyst used. With catalytic amounts of copper and air, 3-oxocyclohexane carboxylic acid is formed preferentially, but when using an excess of copper, the chlorinated product is obtained in higher yields. This reaction occurs because the orthoformic carbon atom has a greater electron density than the meta formic carbon atom. The reaction mechanism begins with oxidation of the metal to form a metal oxide which then reacts with CO to produce CO2 and H2O.</p>Formula:C7H10O3Purity:Min. 95%Molecular weight:142.15 g/mol2-Methyl-4-(naphthalen-2-yl)-4-oxobutanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C15H14O3Purity:Min. 95%Molecular weight:242.27 g/mol4-(1H-Pyrazol-1-yl)phenol
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8N2OPurity:Min. 95%Molecular weight:160.17 g/molethyl 3-[(propan-2-yl)amino]propanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H17NO2Purity:Min. 95%Molecular weight:159.2 g/molN-Methyl-3-phenyl-1,2,4-oxadiazol-5-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H9N3OPurity:Min. 95%Molecular weight:175.19 g/mol(2-Isothiocyanatopropyl)benzene
CAS:Versatile small molecule scaffoldFormula:C10H11NSPurity:Min. 95%Molecular weight:177.27 g/molMethyl 5-bromomethyl-2-chlorobenzoate
CAS:<p>Methyl 5-bromomethyl-2-chlorobenzoate is a cytotoxic agent that inhibits tumor growth. It is a potent inhibitor of the enzyme PARP-1, which is involved in DNA repair, and inhibits tumor growth in vivo. Methyl 5-bromomethyl-2-chlorobenzoate is also able to complex with temozolomide and potentiate its antitumor activity. This drug has been shown to inhibit tumor growth in xenograft models, including xenografts of human non-small cell lung cancer cells transplanted into mice.</p>Formula:C9H8BrClO2Purity:Min. 95%Molecular weight:263.52 g/molThieno[3,2-d]pyrimidine-4-thiol
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H4N2S2Purity:Min. 95%Molecular weight:168.2 g/mol4-Hydrazinothieno[3,2-d]pyrimidine
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H6N4SPurity:Min. 95%Molecular weight:166.21 g/mol2-Chloro-N-(2-cyanoethyl)-N-(4-methylphenyl)acetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13ClN2OPurity:Min. 95%Molecular weight:236.7 g/mol2-Chloro-N-(2-cyanoethyl)-N-phenylacetamide
CAS:Versatile small molecule scaffoldFormula:C11H11ClN2OPurity:Min. 95%Molecular weight:222.67 g/mol2-Chloro-N-(2-cyanoethyl)-N-(2-methoxyphenyl)acetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13ClN2O2Purity:Min. 95%Molecular weight:252.69 g/molThieno[3,2-d]pyrimidin-4(1H)-one
CAS:<p>Thieno[3,2-d]pyrimidin-4(1H)-one is a synthetic compound that has been shown to inhibit cancer cell proliferation. It has an amination reaction at the 2' position of the pyrimidine ring and this pharmacophore is responsible for its anticancer activity. Thieno[3,2-d]pyrimidin-4(1H)-one inhibits leukemia HL-60 cells with a potency similar to that of imatinib. It also inhibits hepg2 cells, which are tumor cells derived from hepatocytes. The kinase selectivity profile of thieno[3,2-d]pyrimidin-4(1H)-one does not show any toxicity towards normal cells such as human skin fibroblasts or human umbilical vein endothelial cells. Thieno[3,2-d]pyrimidin-4(1H)-one exhibits a safety profile similar</p>Formula:C6H4N2OSPurity:Min. 95%Molecular weight:152.17 g/mol1-{Thieno[3,2-d]pyrimidin-4-yl}pyrrolidine
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11N3SPurity:Min. 95%Molecular weight:205.28 g/mol3-Amino-8-methyl-1,3-diazaspiro[4.5]decane-2,4-dione
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H15N3O2Purity:Min. 95%Molecular weight:197.23 g/mol
![2-[(4-Methanesulfonylphenyl)sulfanyl]benzoic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA18513.webp&w=3840&q=75)
![1-Chloro-4-[(2-chloroethyl)sulfonyl]benzene](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA19184.webp&w=3840&q=75)
![7-Methylpyrazolo[1,5-a]pyridine-3-carboxylic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA20547.webp&w=3840&q=75)
![ethyl 3-[(propan-2-yl)amino]propanoate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA21722.webp&w=3840&q=75)
![Thieno[3,2-d]pyrimidine-4-thiol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA22924.webp&w=3840&q=75)
![4-Hydrazinothieno[3,2-d]pyrimidine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA22926.webp&w=3840&q=75)
![Thieno[3,2-d]pyrimidin-4(1H)-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA23410.webp&w=3840&q=75)
![1-{Thieno[3,2-d]pyrimidin-4-yl}pyrrolidine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA23448.webp&w=3840&q=75)
![3-Amino-8-methyl-1,3-diazaspiro[4.5]decane-2,4-dione](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FRAA25293.webp&w=3840&q=75)