Building Blocks
Subcategories of "Building Blocks"
- Boronic Acids & Boronic Acid Derivatives(5,781 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,101 products)
- Organic Building Blocks(61,033 products)
Found 205320 products of "Building Blocks"
Pyrazolo[3,2-c][1,2,4]triazin-4-ol
CAS:Versatile small molecule scaffoldFormula:C5H4N4OPurity:Min. 95%Molecular weight:136.11 g/mol6-Bromo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
CAS:Versatile small molecule scaffoldFormula:C10H10BrNOPurity:Min. 95%Molecular weight:240.1 g/moltert-Butyl 3-phenoxyazetidine-1-carboxylate
CAS:Tert-butyl 3-phenoxyazetidine-1-carboxylate is a boronate ester that can be used in the coupling of arylboronic acids. It reacts with aryl halides or triflates to form a new carbon-carbon bond. This reaction proceeds through the formation of an intermediate, phenoxyacetylene. The tertiary alcohol group on the tert-butyl 3-phenoxyazetidine-1-carboxylate molecule is then attacked by the carbonyl carbon atom on the phenoxyacetylene intermediate to form a new carbon-carbon bond. This reaction can be catalyzed with palladium and copper catalysis.Formula:C14H19NO3Purity:Min. 95%Molecular weight:249.3 g/mol2-cyclopropyl-1-phenylethan-1-one
CAS:2-Cyclopropyl-1-phenylethan-1-one is a drug that has been used in the treatment of psychosis. It has been shown to have growth regulatory properties and to be able to inhibit the conversion of catecholamines and serotonin into their respective metabolites. 2-Cyclopropyl-1-phenylethan-1-one also decreases the level of dopamine, which can lead to symptoms such as psychosis. This drug is used for the treatment of hypofunction and may be effective in patients with Parkinson's disease who have low levels of dopamine in their brains. 2-Cyclopropyl-1-phenylethan-1-one has been shown to produce a number of hydrosilylation products when reacted with an alkene or alkyne substrate. These reactions are catalyzed by platinum complexes, which often undergo formylation, cyclization, or addition reactions during these processes. The 2-, 3-, 4-, 5-,
Formula:C11H12OPurity:Min. 95%Molecular weight:160.21 g/molMethyl 4-(2-oxopyrrolidin-1-yl)butanoate
CAS:Versatile small molecule scaffoldFormula:C9H15NO3Purity:Min. 95%Molecular weight:185.22 g/molEthyl 1-Oxo-2,3-Dihydro-1H-Indene-2-Carboxylate
CAS:Ethyl 1-Oxo-2,3-dihydro-1H-indene-2-carboxylate is an organic compound which is an envisaged dicarbonyl. It is also a reagent in the synthesis of naphthoquinones and aldol condensation. It has been used as a tosylating agent and diazo transfer agent. The crystal structure of this compound was determined by XRD analysis.Formula:C12H12O3Purity:Min. 95%Molecular weight:204.22 g/mol2-(1-Oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetic acid
CAS:Versatile small molecule scaffoldFormula:C12H12O3Purity:Min. 95%Molecular weight:204.2 g/mol3,7,11-Trimethyldodecan-1-ol
CAS:Versatile small molecule scaffoldFormula:C15H32OPurity:Min. 95%Molecular weight:228.41 g/mol5-(Methoxycarbonyl)furan-2-carboxylic acid
CAS:5-(Methoxycarbonyl)furan-2-carboxylic acid is a chemical that can be used as a feedstock for the production of chemicals such as polymers, plastics, and pharmaceuticals. It can be synthesized using an oxidation process involving 5-methoxybenzoic acid as a substrate.Formula:C7H6O5Purity:Min. 95%Molecular weight:170.12 g/mol2-Bromoresorcinol
CAS:2-Bromoresorcinol is a carbonyl compound that has been shown to inhibit farnesyltransferase, an enzyme that mediates the transfer of farnesyl groups. The inhibition of this enzyme leads to a decrease in the production of lipids and other substances essential for cancer cell growth. 2-Bromoresorcinol also inhibits the production of furocoumarins by hydroxide solution, trifluoromethanesulfonic acid, and sodium hydroxide solution. This product can be used as a synthetic intermediate for the synthesis of drugs such as benzofuran derivatives.Formula:C6H5BrO2Purity:Min. 95%Molecular weight:189.01 g/mol2-Methylquinoline-4-carbaldehyde
CAS:Versatile small molecule scaffold
Formula:C11H9NOPurity:Min. 95%Molecular weight:171.19 g/mol9-azabicyclo[3.3.1]nonane hcl
CAS:9-azabicyclo[3.3.1]nonane hcl is an aliphatic, alcohol oxidant that has radical mechanism and is mediated by hydroxylamine. It can be used in the oxidation of benzyl alcohol to benzaldehyde. This compound also has a catalytic effect on the oxidation of 5-hydroxytryptamine (5-HT) to 5-hydroxyindoleacetic acid (5-HIAA). The product may be used in pharmaceuticals, such as the treatment of depression or anxiety, as well as in oxidations involving aliphatic alcohols. The activation energy for this reaction is 32 kcal/mol at 25°C and atmospheric pressure.Formula:C8H16ClNPurity:Min. 95%Molecular weight:161.67 g/molD-Xylopyranose
CAS:D-Xylopyranose is a sugar with the chemical formula C5H10O5. It is a potent antagonist of sweet taste, which may be due to its ability to bind to the sweet receptor on the tongue. D-Xylopyranose can also be used as an analytical reagent in analytical chemistry and has been shown to have anti-inflammatory properties. D-Xylopyranose can be hydrolyzed by acid or base into two molecules of l-arabinose and one molecule of water, and is composed of five carbon atoms, 10 hydrogen atoms, one oxygen atom, and one hydroxyl group. The structure of D-xylopyranose contains a terminal residue (e.g., l-arabinose) that can form glycosidic bonds with other sugars such as glucose or sucrose to form disaccharides such as maltose or sucrose.Formula:C5H10O5Purity:Min. 95%Molecular weight:150.13 g/mol5-Phenyl-1H-imidazol-2-amine
CAS:5-Phenyl-1H-imidazol-2-amine is a marine alkaloid that has been shown to have antibacterial activity. It is active against both Gram-positive and Gram-negative bacteria, as well as fungi. 5-Phenyl-1H-imidazol-2-amine has also been shown to inhibit the growth of Escherichia coli and Staphylococcus aureus. This compound is not active against Sarcina lutea, Enterobacter cloacae, Pseudomonas aeruginosa, Proteus vulgaris, or Klebsiella pneumoniae.
Formula:C9H9N3Purity:Min. 95%Molecular weight:159.19 g/mol2-Chloro-m-xylene
CAS:2-Chloro-m-xylene is a nucleophilic reagent that is used for the Suzuki coupling reaction. It reacts with amines to produce chloroalkyl amines and can be used as a cross-coupling agent for the synthesis of halides or palladium complexes. 2-Chloro-m-xylene has been shown to react with chloride ion to form an optimal reaction, which proceeds at low temperature, in the presence of copper chloride. The chlorine atom in this compound is very reactive and has a nucleophilic nature, which allows it to react with other molecules. This property makes 2-chloro-m-xylene an excellent reagent for the synthesis of organic compounds.Formula:C8H9ClPurity:Min. 95%Molecular weight:140.61 g/mol4,5,6,7-Tetrahydro-1H-1,2,3-benzotriazole
CAS:Versatile small molecule scaffoldFormula:C6H9N3Purity:Min. 95%Molecular weight:123.16 g/mol1,4-Dioxa-8-azaspiro[4.5]decan-7-one
CAS:Versatile small molecule scaffoldFormula:C7H11NO3Purity:Min. 95%Molecular weight:157.17 g/mol(Butan-2-yl)thiourea
CAS:Versatile small molecule scaffoldFormula:C5H12N2SPurity:Min. 95%Molecular weight:132.23 g/mol4-Amino-1H-pyrazolo[3,4-d]pyrimidine-3-carbonitrile
CAS:Versatile small molecule scaffoldFormula:C6H4N6Purity:Min. 95%Molecular weight:160.14 g/mol3-Hydroxy-4-phenylbutanoic acid
CAS:3-Hydroxy-4-phenylbutanoic acid is a chemical compound that is used in the synthesis of medicines. It is a stereospecific, water soluble, and soluble form of butyric acid. 3-Hydroxy-4-phenylbutanoic acid can be synthesized by Streptomyces coelicolor through biosynthesis. This process involves two steps: the first step is the synthesis of butyryl coenzyme A from acetone and acetoacetate; and the second step is the conversion of butyryl coenzyme A to 3-(3-hydroxyphenyl)-4-(1,1,2,2,-tetrafluoroethyl)butyric acid. The use of this compound as a carbon source in high temperature cultures has been shown to increase production of other metabolites such as antibiotics.
Formula:C10H12O3Purity:Min. 95%Molecular weight:180.2 g/mol
![Pyrazolo[3,2-c][1,2,4]triazin-4-ol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FGAA72665.webp&w=3840&q=75)
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