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(61,037 products)
Found 196200 products of "Building Blocks"
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1-{4-[(4-Methylphenyl)methoxy]phenyl}propan-2-amine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C17H22ClNOPurity:Min. 95%Molecular weight:291.8 g/mol3-Methoxy-3-phenylazetidine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H14ClNOPurity:Min. 95%Molecular weight:199.68 g/mol6-[(Difluoromethyl)sulfanyl]-1,2,3,4-tetrahydronaphthalen-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H10F2OSPurity:Min. 95%Molecular weight:228.26 g/mol5-Chloro-N,N-dimethyl-1,2,4-thiadiazol-3-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H6ClN3SPurity:Min. 95%Molecular weight:163.63 g/mol1-Hydroxy-4-methylcyclohexane-1-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H14O3Purity:Min. 95%Molecular weight:158.19 g/mol2-Hydroxybicyclo[2.2.1]heptane-2-carboxylic acid
CAS:<p>2-Hydroxybicyclo[2.2.1]heptane-2-carboxylic acid is an aralkyl compound that is an active substance in a reaction of the Diels-Alder type. It can also be used as a starting material for the synthesis of other compounds. The compound is oxidized to 2,3-dihydroxybicyclo[2.2.1]heptane carboxylic acid, which reacts with sodium hypochlorite and hydrogen gas to form 2,3-dihydroxybicyclo[2.2.1]heptane 1,4-oxazepine 4,5-dicarboxylic acid and hydrogen chloride gas. This process is called oxidative decarboxylation and it can be used as an analytical technique for determining the concentration of the original compound in a sample. Optically active 2-hydroxybicyclo</p>Formula:C8H12O3Purity:Min. 95%Molecular weight:156.18 g/mol5-{[4-(Dimethylamino)phenyl]methylidene}-2-sulfanylideneimidazolidin-4-one
CAS:<p>5-{[4-(Dimethylamino)phenyl]methylidene}-2-sulfanylideneimidazolidin-4-one is a reagent that can be used in the spectrophotometric measurement of metal ions. This reagent is a colorless solid that can be used as a solvent for metal ions. 5-{[4-(Dimethylamino)phenyl]methylidene}-2-sulfanylideneimidazolidin-4-one will react with the metal ion to form a complex, which will absorb light at specific wavelengths depending on the type of metal ion and its concentration. The stoichiometric constant and photometric constant are related to the wavelength of light absorbed by the complex formed from the reagent and metal ion.</p>Formula:C12H13N3OSPurity:Min. 95%Molecular weight:247.32 g/mol1-Chloro-4-iodo-2-nitrobenzene
CAS:<p>1-Chloro-4-iodo-2-nitrobenzene is a sulfone molecule that is synthesized by the reaction of piperazine with nitrous acid. It has been shown to have antagonistic activities against the 5-HT6 receptor, which contributes to its antiemetic properties. 1-Chloro-4-iodo-2-nitrobenzene is also able to inhibit the growth of cells in culture and has been used as a tool in crystallography studies.</p>Formula:C6H3ClINO2Purity:Min. 95%Molecular weight:283.45 g/mol1-Iodo-2-methyl-3-nitrobenzene
CAS:<p>1-Iodo-2-methyl-3-nitrobenzene is an acylated, formylated, plant growth inhibitor. It is used as a herbicide to control weeds and grasses. 1-Iodo-2-methyl-3-nitrobenzene does not affect the roots of plants but instead inhibits their growth by inhibiting enzymes involved in formylation and acylation. The inhibition of these enzymes prevents the formation of proteins necessary for cell division and plant development.</p>Formula:C7H6INO2Purity:Min. 95%Molecular weight:263.03 g/mol3-(Propan-2-yloxy)propanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H12O3Purity:Min. 95%Molecular weight:132.16 g/mol1-[(2-Chloroethyl)sulfanyl]pentane
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H15ClSPurity:Min. 95%Molecular weight:166.71 g/mol1-Methyl-3-[(4-methylphenyl)amino]pyrrolidine-2,5-dione
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H14N2O2Purity:Min. 95%Molecular weight:218.25 g/mol4-amino-3-nitrobenzamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H7N3O3Purity:Min. 95%Molecular weight:181.15 g/mol4-(Methylamino)-3-nitrobenzamide
CAS:<p>4-(Methylamino)-3-nitrobenzamide is a chemical compound that is synthesized by the reaction of methylamine with sodium chloride in the presence of thionyl chloride. The yield of this product is high and it can be used as a precursor for other compounds, such as pharmaceuticals.</p>Formula:C8H9N3O3Purity:Min. 95%Molecular weight:195.18 g/molN-Methyl-4-(methylao)-3-nitrobenzamide
CAS:<p>N-Methyl-4-(methylao)-3-nitrobenzamide is a thionyl chloride derivative that is produced by reacting with methylamine and nitrobenzoyl chloride. It is a synthetic compound that has been used in the synthesis of other organic compounds. The product yield can be increased by reacting the reagents under higher temperature conditions.</p>Formula:C9H11N3O3Purity:Min. 95%Molecular weight:209.2 g/mol(5,7-Dimethyl-[1,2,4]triazolo[4,3-a]pyrimidin-3-ylsulfanyl)-acetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10N4O2SPurity:Min. 95%Molecular weight:238.27 g/mol3-Hydroxy-5-phenylpyrazine-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H8N2O3Purity:Min. 95%Molecular weight:216.19 g/mol2-Chloro-6-phenylpyrazine
CAS:<p>2-Chloro-6-phenylpyrazine is an organic compound with the formula (C6H5)2ClN. It is a palladium catalyst, used in cross-coupling reactions. It reacts with aryl halides and amides to give substituted pyridines. The reaction mechanism involves initial formation of an arene palladacycle that undergoes nucleophilic attack by the nucleophile, followed by elimination of chloride, to give the product amide. 2-Chloro-6-phenylpyrazine is also a starting material for the synthesis of heterocycles such as pyrazoles and pyridazines, which play important roles in pharmaceuticals and agrochemicals.</p>Formula:C10H7ClN2Purity:Min. 95%Molecular weight:190.63 g/mol2-Chloro-5,6-diphenylpyrazine
CAS:<p>2-Chloro-5,6-diphenylpyrazine is a potent, selective inhibitor of the prostacyclin receptor (IP). The IC50 is 0.3 μM and it has a Ki value of 4.1 μM. 2-Chloro-5,6-diphenylpyrazine has been shown to inhibit cancer cell proliferation in vitro and in vivo. It inhibits the growth of colon cancer cells HCT116 with an IC50 of 5 μM when used at a concentration of 10 μM or higher. 2-Chloro-5,6-diphenylpyrazine also inhibits the growth of prostate cancer cells PC3 with an IC50 of 7 μM when used at a concentration of 10 μM or higher.</p>Formula:C16H11ClN2Purity:Min. 95%Molecular weight:266.72 g/mol3-Phenylpyrazin-2-amine
CAS:<p>3-Phenylpyrazin-2-amine is a synthetic compound that has been used in a variety of techniques, such as chromatographic separations and nucleophilic attack. It can be synthesized by dehydrogenative coupling of an aldehyde with an amide. The compound can also be synthesized from 3-phenylpyrazine-2-carboxylic acid and ammonia in the presence of sulfuric acid. The synthesis of 3-phenylpyrazin-2-amine can also be achieved by the reaction of phenylhydrazine with formamide or acetaldehyde. 3-Phenylpyrazin-2-amine has been studied for its receptor binding and was found to bind to dopamine receptors in the bovine serum albumin (BSA). This compound is orally active and effective at doses below 100mg/kg body weight.</p>Formula:C10H9N3Purity:Min. 95%Molecular weight:171.2 g/mol
