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"
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5-[2-(Benzenesulfonyl)ethyl]-1H-indole
CAS:<p>5-[2-(Benzenesulfonyl)ethyl]-1H-indole is a chemical compound that contains a nitro group, which is a functional group consisting of a nitrogen atom double-bonded to an oxygen atom. It has been shown to be useful for the synthesis of acetylpyridine derivatives. The synthesis of this compound involves the reaction of indole with 2-chloroethanol and benzenesulfonyl chloride in the presence of sodium hydroxide. This product can also be prepared by reacting chlorination with an alkylamine and nitric acid. 5-[2-(Benzenesulfonyl)ethyl]-1H-indole can be used as a precursor for intermediates in the synthesis of sulphones and salifying agents that are used for polymerization reactions.</p>Formula:C16H15NO2SPurity:Min. 95%Molecular weight:285.4 g/mol6-(Morpholin-4-yl)-2,3-dihydro-1H-indole dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H18Cl2N2OPurity:Min. 95%Molecular weight:277.2 g/mol2-{[2-(4-Aminophenyl)ethyl]amino}ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H16N2OPurity:Min. 95%Molecular weight:180.25 g/mol5H,6H,7H,8H-Imidazo[1,2-a]pyridine-2-carbohydrazide
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H12N4OPurity:Min. 95%Molecular weight:180.21 g/mol1-Bromo-4-(1,1,1-trifluoro-2-methylpropan-2-yl)benzene
CAS:Versatile small molecule scaffoldFormula:C10H10BrF3Purity:Min. 95%Molecular weight:267.1 g/molPteridine-2,4-diamine
CAS:<p>Pteridine-2,4-diamine is a peroxide that is found in nature. It has been shown to have an inhibitory effect on mutant enzymes that are involved in the production of hydrogen peroxide. Pteridine-2,4-diamine binds to a ligand and prevents it from reacting with hydrogen peroxide. This compound is used as a surfactant in pharmaceutical preparations. It also has an inhibitory effect on soybean lipoxygenase, which may be due to its ability to bind to the phosphonium salt at the active site and prevent the catalytic reaction with hydrogen peroxide.</p>Formula:C6H6N6Purity:Min. 95%Molecular weight:162.15 g/molEthyl (1S,2R/1R,2S)-2-aminocyclohexanecarboxylate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H18ClNO2Purity:Min. 95%Molecular weight:207.7 g/molDimethyl cyclobut-1-ene-1,2-dicarboxylate
CAS:<p>Dimethyl cyclobut-1-ene-1,2-dicarboxylate (DMCB) is a lipase inhibitor that belongs to the class of dicarboxylic acid esters. It is used as an immobilized catalyst in organic synthesis and has a high stereoselectivity. This compound has been shown to be effective in catalyzing the thermal isomerization of maleates to produce 1,2-diols with high yields. DMCB also has a spontaneous reaction with photosensitizers such as rose bengal and benzoporphyrin derivative. The maleate form can be converted into the diacid form by the enzyme maleate dehydrogenase, which is found in porcine tissues. The diacid form can then undergo hydrolysis by an esterase or glucuronidase, releasing DMCB and regenerating the original maleate substrate.</p>Formula:C8H10O4Purity:Min. 95%Molecular weight:170.16 g/mol2-Hydrazinyl-5-nitropyrimidin-4-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H6N6O2Purity:Min. 95%Molecular weight:170.13 g/mol5-Acetylbenzothiophene
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H8OSPurity:Min. 95%Molecular weight:176.23 g/mol4-tert-Butylcyclohexa-3,5-diene-1,2-dione
CAS:<p>4-tert-Butylcyclohexa-3,5-diene-1,2-dione is a flavonoid that inhibits the enzyme tyrosinase in the synthesis of melanin. It is used for the treatment of hyperpigmentation conditions, such as melasma and chloasma. The inhibitory effect of 4-tert-Butylcyclohexa-3,5-diene-1,2-dione has been shown to be competitive with respect to 3-hydroxyanthranilic acid and noncompetitive with respect to naphthol. 4BCD also inhibits the monophenolase activity of tyrosinase and its ability to oxidize phenols. This inhibition is due to its structural similarity with phenols and its ability to bind covalently with tyrosinase's active site.</p>Formula:C10H12O2Purity:90%NmrColor and Shape:PowderMolecular weight:164.2 g/mol(3-Methylbutoxy)benzene
CAS:<p>(3-Methylbutoxy)benzene is a cyclic monomer that can be used in the production of polyester plastics. It has been shown to polymerize with isopentyl by means of an initiator. This reaction system produces a polymerized polymer. The phenyl group in this molecule has been shown to interact with eugenol through transition-state profile and reaction system studies, as well as polymerization reactions with benzene. The fluorescent properties of this compound make it suitable for use in fluorescent labelling of proteins and DNA.</p>Formula:C11H16OPurity:Min. 95%Molecular weight:164.24 g/mol1-Cyano-cyclohexanecarboxylic acid ethyl ester
CAS:<p>1-Cyano-cyclohexanecarboxylic acid ethyl ester is a synthetic intermediate in the preparation of benzene. It is used as a reagent for the synthesis of methylcyclohexane and other cyclohexanones. The compound can be prepared by reacting chlorinated aliphatic hydrocarbons with carbon dioxide, followed by acidification and decarbonylation. 1-Cyano-cyclohexanecarboxylic acid ethyl ester can be purified by distillation or recrystallization from acetonitrile, chloroform, or benzene.</p>Formula:C10H15NO2Purity:Min. 95%Molecular weight:181.23 g/mol3-(2-Fluorophenyl)but-2-enoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H9FO2Purity:Min. 95%Molecular weight:180.17 g/molPhenylsuccinic anhydride
CAS:<p>Phenylsuccinic anhydride is a reactive, receptor binding, expressed, polycarboxylic acid that has nitrogen atoms. It can be used as an anticancer agent and has shown anticancer activity against α7 nicotinic acetylcholine receptors in the central nervous system. Phenylsuccinic anhydride is also used for the preparation of fluorinated anhydrides for use in nonaqueous solvents.</p>Formula:C10H8O3Purity:Min. 95%Molecular weight:176.17 g/molMethyl 3-amino-6-bromo-5-methylpyrazine-2-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8BrN3O2Purity:Min. 95%Molecular weight:246.06 g/mol6-Amino-2-methyl-quinolin-4-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10N2OPurity:Min. 95%Molecular weight:174.2 g/mol4-Methyl-3-phenylpentanenitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H15NPurity:Min. 95%Molecular weight:173.3 g/mol3,5-Di-tert-butyl-1H-pyrazole
CAS:<p>3,5-Di-tert-butyl-1H-pyrazole is a molecule that has two phenyl groups and one hydrogen bond. It is used as a reagent in analytical chemistry for the determination of hydrochloric acid and in crystallography for the study of x-ray crystal structures. 3,5-Di-tert-butyl-1H-pyrazole has been shown to have x-ray crystal structures with four nitrogens and one proton. The molecule also has a pyrazole ring at the center that contains one hydroxy group and two phenyl groups. The molecular weight of 3,5-Di-tert-butyl-1H-pyrazole is 152.2 g/mol.</p>Formula:C11H20N2Purity:Min. 95%Molecular weight:180.29 g/mol4-N-Propylbenzenesulfonamide
CAS:<p>4-N-Propylbenzenesulfonamide is a hydrophobic compound that binds to the active site of carbonyl reductase, an enzyme involved in the metabolism of ketones and aldehydes. It also inhibits the catalytic activity of this enzyme, which reduces the amount of carbonyls produced in the cell. 4-N-Propylbenzenesulfonamide has been shown to be effective in preventing kidney damage in animal models. The structural features of this drug are similar to those found in acetoacetate and propionate, which are important for stimulating renal function. These drugs can bind to alpha and beta subunits on the surface of renal tubules, resulting in increased blood flow, improved filtration rates, and decreased fluid retention. This leads to protection against acute kidney injury (AKI) and chronic kidney disease (CKD).</p>Formula:C9H13NO2SPurity:Min. 95%Molecular weight:199.27 g/mol
