31408-56-7

Basic information

• Product Name: 2-[(2-chlorobenzoyl)amino]benzoic acid
• Synonyms: 2-[(2-chlorobenzoyl)amino]benzoic acid
• CAS NO: 31408-56-7
• Molecular Formula: C₁₄H₁₀ClNO₃
• Molecular Weight: 275.69
• Mol File: 31408-56-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(2-chlorobenzoyl)amino]benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-chlorobenzoyl)amino]benzoic acid(31408-56-7)
• EPA Substance Registry System: 2-[(2-chlorobenzoyl)amino]benzoic acid(31408-56-7)

Safety Data

• Hazardous Substances Data: 31408-56-7(Hazardous Substances Data)

Upstream product

• 609-65-4 o-chlorobenzoyl chloride 
• 118-92-3 anthranilic acid 
• 123-00-2 4-(3-Aminopropyl)morpholine 
• 552-16-9 ortho-nitrobenzoic acid 
• 118-91-2 ortho-chlorobenzoic acid 
• 4765-51-9 2-(2-chlorophenyl)benzo[d]1,3-oxazin-4-one 

Downstream Products

• 4765-51-9 2-(2-chlorophenyl)benzo[d]1,3-oxazin-4-one 
• 92161-79-0 3-amino-2-(2-chlorophenyl)quinazolin-4(3H)-one 

Relevant articles and documents

Precursor-directed combinatorial biosynthesis of cinnamoyl, dihydrocinnamoyl, and benzoyl anthranilates in saccharomyces cerevisiae

Biological synthesis of pharmaceuticals and biochemicals offers an environmentally friendly alternative to conventional chemical synthesis. These alternative methods require the design of metabolic pathways and the identification of enzymes exhibiting ade

Traceless synthesis of 3H-quinazolin-4-ones via a combination of solid-phase and solution methodologies

A solid-phase traceless synthesis of quinazolin-4-ones is described. An aldehyde functionalized resin was reductively aminated with primary amines, and the resin-bound secondary amine acylated with o-nitro-benzoic acids. The nitro group was reduced with tin(II) chloride, and the aniline acylated with acid anhydrides. Acidolytic cleavage afforded a diamide, which was cyclized in solution phase to the 3H-quinazolin-4-one removing the trace of the linker.