68506-37-6

Basic information

• Product Name: 2-(2-nitrobenzamido)benzoic acid
• Synonyms: 2-(2-nitrobenzamido)benzoic acid
• CAS NO: 68506-37-6
• Molecular Weight: 286.244
• Mol File: 68506-37-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(2-nitrobenzamido)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-nitrobenzamido)benzoic acid(68506-37-6)
• EPA Substance Registry System: 2-(2-nitrobenzamido)benzoic acid(68506-37-6)

Safety Data

• Hazardous Substances Data: 68506-37-6(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 610-14-0 2-nitrobenzyl chloride 
• 134-20-3 2-carbomethoxyaniline 
• 49854-16-2 methyl 2-(2-aminobenzoylamino)benzoate 
• 7501-38-4 2-(2'-nitrophenyl)-3,1-benzoxazin-4-one 
• 37960-65-9 potassium anthranilate 
• 72367-10-3 2-(2-nitrobenzoylamino)benzoic acid methyl ester 

Downstream Products

• 612-34-0 N-anthraniloyl-anthranilic acid 
• 7501-38-4 2-(2'-nitrophenyl)-3,1-benzoxazin-4-one 
• 875017-11-1 2-nitro-N-(2-(pyrrolidine-1-carbonyl)phenyl)benzamide 
• 1404368-81-5 (S)-1-(2-(2-acetamidobenzamido)benzoyl)-N-methylpyrrolidine-2-carboxamide 
• 1404368-82-6 (S)-N-methyl-1-(2-(2-nitrobenzamido)benzoyl)pyrrolidine-2-carboxamide 
• 1404368-83-7 (S)-N-tert-butyl-1-(2-(2-nitrobenzamido)benzoyl)pyrrolidine-2-carboxamide 
• 1404368-84-8 (S)-N-(4-bromophenyl)-1-(2-(2-nitrobenzamido)benzoyl)pyrrolidine-2-carboxamide 
• 1404368-85-9 2-acetamido-N-(2-(pyrrolidine-1-carbonyl)phenyl)benzamide 
• 1448441-17-5 (R)-methyl 2-(2-(1-(2-(2-nitrobenzamido)benzoyl)pyrrolidine-2 carboxamido)benzamido)benzoate 
• 1448441-18-6 (R)-1-(2-(2-aminobenzamido)benzoyl)-N-(2-((2-(methylcarbamoyl)phenyl)carbamoyl)phenyl)pyrrolidine-2-carboxamide 
• 1448441-08-4 (R)-1-(2-(2-((2-bromopropan-2-yl)amino)benzamido)benzoyl)-N-(2-((2-(methylcarbamoyl)phenyl)carbamoyl)phenyl) pyrrolidine-2-carboxamide 
• 25380-15-8 2-(4-oxo-4H-quinazolin-3-yl)benzoic acid 
• 316142-99-1 2-nitro-N-(2-(phenylcarbamoyl)phenyl)benzamide 
• 49854-16-2 methyl 2-(2-aminobenzoylamino)benzoate 

Relevant articles and documents

A synthetic zipper peptide motif orchestrated via co-operative interplay of hydrogen bonding, aromatic stacking, and backbone chirality

Here, we report on a new class of synthetic zipper peptide which assumes its three-dimensional zipper-like structure via a co-operative interplay of hydrogen bonding, aromatic stacking, and backbone chirality. Structural studies carried out in both solid- and solution-state confirmed the zipper-like structural architecture assumed by the synthetic peptide which makes use of unusually remote inter-residual hydrogen-bonding and aromatic stacking interactions to attain its shape. The effect of chirality modulation and the extent of noncovalent forces in the structure stabilization have also been comprehensively explored via single-crystal X-ray diffraction and solution-state NMR studies. The results highlight the utility of noncovalent forces in engineering complex synthetic molecules with intriguing structural architectures.

One dimensional unichemo protection (UCP) in organic synthesis

A protected template molecule and a new one-dimensional UniChemo Protection (UCP) organic synthetic method for preparing polyfunctional organic molecules is described. The synthetic method can be used with many kinds of chemical reactions and provides selective access to many functional groups in a template molecule. The method utilizes protection groups that are each composed of building block units that can be removed one by one affording a new protection group one unit shorter or exposing a functional group on the template molecule. The exposed functional group on the template molecule can react with a target group. Different target groups can be introduced into the template molecule by using protection groups containing different numbers of building block units.