124842-39-3

Basic information

• Product Name: [(3-{[(carboxymethyl)amino]carbonyl}benzoyl)amino]acetic acid
• Synonyms: [(3-{[(carboxymethyl)amino]carbonyl}benzoyl)amino]acetic acid
• CAS NO: 124842-39-3
• Molecular Weight: 280.237
• Mol File: 124842-39-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: [(3-{[(carboxymethyl)amino]carbonyl}benzoyl)amino]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [(3-{[(carboxymethyl)amino]carbonyl}benzoyl)amino]acetic acid(124842-39-3)
• EPA Substance Registry System: [(3-{[(carboxymethyl)amino]carbonyl}benzoyl)amino]acetic acid(124842-39-3)

Safety Data

• Hazardous Substances Data: 124842-39-3(Hazardous Substances Data)

Upstream product

• 56-40-6 glycine 
• 99-63-8 benzene-1,3-dicarbonyl dichloride 
• 121-91-5 isophthalic acid 
• 61202-04-8 [3-(methoxycarbonylmethyl-carbamoyl)-benzoylamino]-acetic acid methyl ester 

Downstream Products

• 180044-88-6 C₂₆H₁₆N₂O₄ 
• 180044-89-7 C₂₈H₂₀N₂O₆ 

Relevant articles and documents

Pseudopeptidic ligands: Exploring the self-assembly of isophthaloylbisglycine (H2IBG) and divalent metal ions

We present a systematic study of the complexation of the new pseudopeptidic ligand isophthaloylbisglycine (H2IBG) with divalent metal ions of varying ionic radius. This work represents the initial employment of H 2IBG in the coordina

DNA binding, solubility, and partitioning characteristics of extended lexitropsins

Four new ligands that bind to the minor groove of DNA have been designed, synthesized, and evaluated by DNA footprinting. Two of the ligands are polyamides containing central regions with five or six N-methylpyrrole units, conferring hydrophobicity and go

Platelet aggregation inhibiting and anticoagulant effects of oligoamines, XVIII: Oligoamines with fluorescent properties, Part B: Fluorophores in the molecular periphery

Seventeen N,N'-benzene-1,3-dimethane and nine N,N',N''-benzene-1,3,5-trimethane derivatives with fluorescent properties have been synthesized. Three of them show antiplatelet activities (inducer collagen, IC50 Borntest) in concentrations 10 μmol/L. They are suitable for interaction studies with biological macromolecules and synthetical and biological membranes. Structure activity relationships demonstrate that heteropolycyclic fluorophores i.e. quinoline, dibenzofurane, or carbazole are favorable substituents for this purpose.