N-Boc-pyrroyl-boronic acid

CAS : 135884-31-0

Ref. 3D-FB18983

Informations sur le produit

• Nom: N-Boc-pyrroyl-boronic acid
• Synonymes: N-Boc-2-pyrroleboronic acid2-Borono-1H-pyrrole-1-carboxylic acid 1-(1,1-dimethylethyl) ester(1-(tert-Butoxycarbonyl)pyrrole-2-yl)b oronic acid, 2-Borono-1H-pyrrole-1-carboxylic acid 1-(1,1-dimethylethyl) ester, N-Boc-2-pyrryl-boronic acid, 1-(t-Butoxycarbonyl)pyrrole-2-boronic acid, 1-(tert-Butoxycarbonyl)-1H-pyrrol-2-ylboronic acid, N-Boc-2-pyrroleboronic acid, 1-Propylpyrrolidine, 1-Boc-pyrrole-2-boronic acid, 1-Boc-2-pyrrolylboronic acid, N-Boc-Pyrrole-2-Boronic Acid, N-Boc-1H-pyrrol-2-ylboronic acid, {1-[(tert-butoxy)carbonyl]-1H-pyrrol-2-yl}boronic acid

Description

N-Boc-pyrroyl-boronic acid is a linker that is used in organic synthesis. It reacts with chloride to form an organochlorine compound, which can be used as an inhibitor of s. aureus or other bacteria. The reaction time for this chemical is shorter than for the corresponding boronic acid, and it does not require the presence of a Lewis acid. This chemical has been shown to have anticancer activity in vitro, and its optimization has been studied using fluorescent carbonyl groups as the active component.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 211.02 g/mol
• Formule: C₉H₁₄BNO₄
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C9H14BNO4/c1-9(2,3)15-8(12)11-6-4-5-7(11)10(13)14/h4-6,13-14H,1-3H3
• Code InChI: InChIKey=ZWGMJLNXIVRFRJ-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)n1cccc1B(O)O