134939-24-5

Basic information

• Product Name: 1H-Pyrrole-2,5-dione, 1-(4-bromophenyl)-3-methyl-
• CAS NO: 134939-24-5
• Molecular Formula: C11H8BrNO2
• Molecular Weight: 266.094
• Mol File: 134939-24-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 1-(4-bromophenyl)-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 1-(4-bromophenyl)-3-methyl-(134939-24-5)
• EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 1-(4-bromophenyl)-3-methyl-(134939-24-5)

Safety Data

• Hazardous Substances Data: 134939-24-5(Hazardous Substances Data)

Upstream product

• 616-02-4 citraconic acid anhydride 
• 106-40-1 4-bromo-aniline 
• 1449799-81-8 (Z)-(4-(4-bromophenylamino)-2-methyl-4-oxo)but-2-enoic acid 
• 80818-24-2 (Z)-(2-methyl-4-(4-nitrophenylamino)-4-oxo)but-2-enoic acid 

Downstream Products

• 25998-51-0 1-(4-bromophenyl)-3-methylpyrrolidine-2,5-dione 
• 1451750-81-4 (3R)-(+)-methyl-N-(4'-bromophenyl)succinimide 
• 873528-72-4 7-(4-bromophenyl)-1-methyl-2,3,7-triazabicyclo[3.3.0]oct-2-ene-6,8-dione 
• 134939-29-0 Dithiocarbonic acid S-[(1S,5S,6S)-3-(4-bromo-phenyl)-7-hex-(Z)-ylidene-1-methyl-2,4-dioxo-3-aza-bicyclo[3.2.0]hept-6-yl] ester O-methyl ester 
• 134939-26-7 Dithiocarbonic acid S-[(3aS,6aR)-2-(4-bromo-phenyl)-3a-methyl-1,3-dioxo-1,2,3,3a,4,6a-hexahydro-cyclopenta[c]pyrrol-5-yl] ester O-methyl ester 
• 134939-25-6 Dithiocarbonic acid S-[(3aR,6aR)-2-(4-bromo-phenyl)-6a-methyl-1,3-dioxo-1,2,3,3a,4,6a-hexahydro-cyclopenta[c]pyrrol-5-yl] ester O-methyl ester 

Relevant articles and documents

Application of maleimide compound as chitin synthase inhibitor

The invention discloses an application of a maleimide compound as shown in a formula I. In the formula I, R0 is phenyl, benzyl, phenethyl, phenylpropyl, p-fluorophenyl, p-chlorophenyl, p-bromophenyl,p-methoxyphenyl, p-methylphenyl or p-hydroxyphenyl, R1 is hydrogen, methyl, phenyl or chlorine; and R2 is hydrogen, methyl, phenyl or chlorine. The provided maleimide compound has a good inhibition effect on chitin synthase.

Effects of chirality on the antifungal potency of methylated succinimides obtained by Aspergillus fumigatus biotransformations. Comparison with racemic ones

Eighteen (3R) and (3R,4R)-N-phenyl-, N-phenylalkyl and N-arylsuccinimides were prepared with high enantioselectivity by biotransformation of maleimides with A. fumigatus. This environmentally friendly, clean and economical procedure was performed by the w