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(61,038 products)
Found 196817 products of "Building Blocks"
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1-Aminopentan-2-one hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H12ClNOPurity:Min. 95%Molecular weight:137.61 g/mol4-Amino-3-phenylbutan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H15NOPurity:Min. 95%Molecular weight:165.23 g/mol7-Methyl-2,3,4,5-tetrahydro-1-benzoxepin-5-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H12O2Purity:Min. 95%Molecular weight:176.21 g/mol5-Bromo-2,3-dihydrobenzofuran-7-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H7BrO3Purity:Min. 95%Molecular weight:243.06 g/mol5-bromo-2-methylpent-1-ene
CAS:<p>5-bromo-2-methylpent-1-ene is an organic compound that belongs to the group of isopentenyl compounds. It is a synthetic compound that has been shown to be effective as an antimicrobial agent. 5-bromo-2-methylpent-1-ene has a copper complex which binds to the copper and diphosphate groups in bacterial DNA, preventing replication and transcription. This drug also inhibits the synthesis of proteins by binding to ribosomes, thereby inhibiting protein synthesis. The antimicrobial activity of 5-bromo-2-methylpent-1e is due to its ability to inhibit RNA synthesis and DNA synthesis in bacteria.</p>Formula:C6H11BrPurity:Min. 95%Molecular weight:163.06 g/mol5-Chloro-1-methyl-2,3-dihydro-1H-indol-2-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8ClNOPurity:Min. 95%Molecular weight:181.62 g/mol2-(Trifluoromethyl)quinolin-7-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H6F3NOPurity:Min. 95%Molecular weight:213.16 g/mol2-Amino-3-bromo-5-chlorobenzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H5BrClNO2Purity:Min. 95%Molecular weight:250.48 g/mol3-(3-fluorophenyl)-2-methylpropanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11O2FPurity:Min. 95%Molecular weight:182.19 g/mol2-Chloro-1-(2,3-dihydro-1H-inden-5-yl)ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H11ClOPurity:Min. 95%Molecular weight:194.66 g/mol2,6,7-Trichloroquinoxaline
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H3Cl3N2Purity:Min. 95%Molecular weight:233.5 g/mol3-Chloro-1-methyl-6-(methylamino)-1,4-dihydropyridazin-4-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H8ClN3OPurity:Min. 95%Molecular weight:173.6 g/mol1-[(2-Methylphenyl)methyl]piperidin-4-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H20N2Purity:Min. 95%Molecular weight:204.31 g/mol3-(1-Benzylpiperidin-4-yl)-1-phenylurea
CAS:<p>Versatile small molecule scaffold</p>Formula:C19H23N3OPurity:Min. 95%Molecular weight:309.4 g/mol1H-Tetrazol-1-ylacetyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C3H3ClN4OPurity:Min. 95%Molecular weight:146.53 g/mol3-(Chloromethyl)-6-methoxypyridazine
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H7ClN2OPurity:Min. 95%Molecular weight:158.58 g/mol2,3-Dimethyl-3H-imidazo[4,5-b]pyridine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9N3Purity:Min. 95%Color and Shape:PowderMolecular weight:147.18 g/molN-Methyl-2-piperidin-1-ylethanamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H18N2Purity:Min. 95%Molecular weight:142.24 g/molH-Imidazo[1,2-a]pyridine-3-carbaldehyde
CAS:<p>H-Imidazo[1,2-a]pyridine-3-carbaldehyde is an anti-infective agent that is active against bacteria and fungi. The compound inhibits the growth of bacteria by interfering with the synthesis of DNA and RNA. H-Imidazo[1,2-a]pyridine-3-carbaldehyde has been shown to be effective in treating infections caused by Stenotrophomonas maltophilia and Pseudomonas aeruginosa. It also has an effect on Enterobacteriaceae, including Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis. H-Imidazo[1,2-a]pyridine-3-carbaldehyde is not effective against Streptococcus species such as Streptococcus pyogenes or Group A beta hemolytic streptococci.</p>Formula:C9H8N2OPurity:Min. 95%Molecular weight:160.17 g/mol2-Hydroxy-3-methoxy-N,N-dimethylbenzamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H13NO3Purity:Min. 95%Molecular weight:195.21 g/mol
