Building Blocks
Subcategorias de "Building Blocks"
- Ácidos Borónicos e Derivados de Ácido Borónico(5.780 produtos)
- Building Blocks Quirais(1.241 produtos)
- Building Blocks Hidrocarbonetos(6.100 produtos)
- Building Blocks orgânicos(61.023 produtos)
Foram encontrados 205289 produtos de "Building Blocks"
(2-Bromo-4-methylphenyl)methanol
CAS:Versatile small molecule scaffold
Fórmula:C8H9BrOPureza:Min. 95%Peso molecular:201.06 g/molN-{8-Cyclopropyl-8-azabicyclo[3.2.1]octan-3-ylidene}hydroxylamine
CAS:Versatile small molecule scaffoldFórmula:C10H16N2OPureza:Min. 95%Peso molecular:180.25 g/mol(1R)-1-(4-Aminophenyl)ethan-1-ol
CAS:Versatile small molecule scaffold
Fórmula:C8H11NOPureza:Min. 95%Peso molecular:137.18 g/mol5-Ethylcyclohex-2-en-1-one
CAS:Versatile small molecule scaffold
Fórmula:C8H12OPureza:Min. 95%Peso molecular:124.18 g/mol2-(4-Methylpiperazin-1-yl)-2-phenylacetic acid
CAS:Versatile small molecule scaffold
Fórmula:C13H18N2O2Pureza:Min. 95%Peso molecular:234.29 g/mol1-Cyclopropylhex-5-en-1-one
CAS:Versatile small molecule scaffold
Fórmula:C9H14OPureza:Min. 95%Peso molecular:138.2 g/molrac-tert-Butyl N-[(1R,3S)-3-(aminomethyl)cyclohexyl]carbamate
CAS:Versatile small molecule scaffold
Fórmula:C12H24N2O2Pureza:Min. 95%Peso molecular:228.33 g/mol1-(3-Bromophenyl)cyclobutan-1-ol
CAS:Versatile small molecule scaffold
Fórmula:C10H11BrOPureza:Min. 95%Peso molecular:227.1 g/molEthyl 4-amino-3-methylbenzoate
CAS:Ethyl 4-amino-3-methylbenzoate is a dimer that can be formed by the reaction of ethyl benzoate with anilines. This dimer has been shown to have an asymmetric center and can form hydrogen bonds with other molecules. The reactivity of this molecule is similar to benzocaine, which is also a dimer, but it does not contain any nitrogen atoms.
Fórmula:C10H13NO2Pureza:Min. 95%Peso molecular:179.22 g/mol3-(1-Hydroxyethyl)benzene-1-sulfonamide
CAS:Versatile small molecule scaffold
Fórmula:C8H11NO3SPureza:Min. 95%Peso molecular:201.25 g/molEthyl 2-(methylsulfanyl)propanoate
CAS:Versatile small molecule scaffold
Fórmula:C6H12O2SPureza:Min. 95%Peso molecular:148.23 g/molN,N-Dimethyl-3-sulfamoylbenzamide
CAS:Versatile small molecule scaffold
Fórmula:C9H12N2O3SPureza:Min. 95%Peso molecular:228.27 g/mol4-(2-Chloroacetyl)benzonitrile
CAS:Versatile small molecule scaffold
Fórmula:C9H6ClNOPureza:Min. 95%Peso molecular:179.6 g/moltert-Butyl 4-(2-methoxy-2-oxo-1-phenylethyl)piperazine-1-carboxylate
CAS:Versatile small molecule scaffold
Fórmula:C18H26N2O4Pureza:Min. 95%Peso molecular:334.4 g/molN-Hydroxy-2-(o-tolyl)acetimidamide
CAS:Versatile small molecule scaffold
Fórmula:C9H12N2OPureza:Min. 95%Peso molecular:164.21 g/mol2-(4-Methoxypyridin-2-yl)acetonitrile
CAS:Versatile small molecule scaffold
Fórmula:C8H8N2OPureza:Min. 95%Peso molecular:148.16 g/mol4-Amino-1-methylpyrimidin-2(1H)-one
CAS:4-Amino-1-methylpyrimidin-2(1H)-one is a chemical compound that belongs to the group of pyrimidine compounds. It has been shown to be an inhibitor of viral life, with its activity against HIV being most well studied. The tautomers of 4-amino-1-methylpyrimidin-2(1H)-one are protonated and stable, meaning that they do not undergo any chemical change in the body. 4-Amino-1-methylpyrimidin-2(1H)-one is also able to form stable complexes with nitrogen atoms. The xray crystal structure for this compound shows that it coordinates with group P2, which contains two nitrogen atoms and one oxygen atom. The interaction between these three atoms is called a dinucleotide phosphate. This group binds to DNA by hydrogen bonds, forming intramolecular hydrogen bonds. The groups on the other side of the molecule bind
Fórmula:C5H7N3OPureza:Min. 95%Peso molecular:125.13 g/mol1-ethynyl-3-(methylthio)benzene
CAS:Versatile small molecule scaffold
Fórmula:C9H8SPureza:Min. 95%Peso molecular:148.23 g/mol2-Aminoperimidine hydrobromide sesquihydrate
CAS:2-Aminoperimidine hydrobromide sesquihydrate (2AP) is a sulfonamide antibiotic that inhibits bacterial growth by binding to the ribosome. 2AP is a potentiometric titrant, with an endpoint of 1.5 M NaOH. It has been shown to inhibit the growth of bacteria, such as Staphylococcus aureus and Escherichia coli, in vitro. The synthesis of 2AP can be achieved through a two-step reaction between ammonium salt and sulfate ester. This chemical synthesis uses the following parameters:
Fórmula:C11H9N3•HBr•(H2O)1Pureza:Min. 95%Peso molecular:291.14 g/mol4-(3,4-Dimethylphenyl)butanal
CAS:Versatile small molecule scaffold
Fórmula:C12H16OPureza:Min. 95%Peso molecular:176.25 g/mol
![N-{8-Cyclopropyl-8-azabicyclo[3.2.1]octan-3-ylidene}hydroxylamine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FMXB16091.webp&w=3840&q=75)
![rac-tert-Butyl N-[(1R,3S)-3-(aminomethyl)cyclohexyl]carbamate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FXNA18641.webp&w=3840&q=75)
