90602-26-9

Usage

Chemical class

Bicyclic compounds derived from heteroaromatic compounds

Molecular weight

301.74 g/mol

Functional groups

Carboxylic acid, ester, and chloro groups

Structure

Contains an azabicyclo[3.2.0]hept-2-ene core with a carboxylic acid group, a 3-chloro substituent, and a 7-oxo (carbonyl) group

Esterification

Phenylmethyl (benzyl) ester of the carboxylic acid group

Applications

Used as a building block in organic synthesis, potential applications in the pharmaceutical industry

Safety precautions

Handle with care, ensure proper safety measures in laboratory settings

Upstream product

• 74476-30-5 benzyl 1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate 

Downstream Products

• 90602-27-0 benzyl 6-(1-hydroxyethyl)-3-chloro-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate 

Relevant academic research and scientific papers

6- and 6,6-disubstituted-3-substituted-1-azabicyclo(3.2.0)hept-2-en-7-one-2-carboxylic acids

Disclosed are 6- and 6,6-disubstituted-3-substituted-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acids (I): STR1 wherein R1 and R2 are, inter alia, independently selected from the group consisting of hydrogen (both are not hydrog

Process for preparing 3-substituted-6-substituted-7-oxo-1-azabicycl(3.2.0)-hept-2-ene-2-carboxylic acid

Disclosed is a process for preparing 3-substituted-thio-6-(1'-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acids (I) STR1 wherein X is a leaving group such as chloro, bromo, tosyl, mesyl or the like; and R8 is, inter alia, sel

Process for preparing 3-substituted-6-substituted-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

Disclosed is a process for preparing 3- and 6-substituted-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acids: STR1 wherein: X is a leaving group such as chloro, bromo, tosyl, mesyl or the like; and R6, R7 and R8 are, i

6- And 6,6-disubstituted-3-substituted amino-1-azabicyclo-[3.2.0]hept-2-en-7-one-2-carboxylic acid

Disclosed are 6- and 6,6-disubstituted-3-substituted amino-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acids (I): STR1 wherein R1 and R2 are, inter alia, independently selected from the group consisting of hydrogen, substituted a

6-(1'-Hydroxyethyl)-3-substituted amino-1-azabicyclo-?3.2.0!hept-2-en-7-one-2-carboxylic acid

Disclosed are 6-(1'-hydroxyethyl)-3-substituted amino-1-azabicyclo?3.2.0!hept-2-en-7-one-2-carboxylic acids (I): STR1 wherein R' and R" are independently selected from H, substituted and unsubstituted alkyl and aralkyl groups, or together form a substitut

3-Halo-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acid

Disclosed is 3-halo-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acid (I): STR1 Such compounds, wherein X is halo, and their pharmaceutically acceptable salt, ester and amide derivatives are useful as antibiotics. Also disclosed are processes for the p

6-(1-Hydroxyethyl)-3-substituted-1-azabicyclo(3.2.0)-hept-2-en-7-one-2-carboxylic acid

Disclosed are 6-(1'-hydroxyethyl)-3-substituted-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acids(I): STR1 wherein X is halo, oxygen (the 2-3 bond is saturated and the species I exists as the carboxylate salt or ester), or --OR wherein R is, inter ali