107313-48-4

Basic information

• Product Name: α-benzamido-β-(2-benzimidazolyl)-L-(-)-propionic acid
• CAS NO: 107313-48-4
• Molecular Weight: 309.324
• Mol File: 107313-48-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: α-benzamido-β-(2-benzimidazolyl)-L-(-)-propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-benzamido-β-(2-benzimidazolyl)-L-(-)-propionic acid(107313-48-4)
• EPA Substance Registry System: α-benzamido-β-(2-benzimidazolyl)-L-(-)-propionic acid(107313-48-4)

Safety Data

• Hazardous Substances Data: 107313-48-4(Hazardous Substances Data)

Upstream product

• 4631-12-3 benzoyl L-aspartic acid 
• 95-54-5 1,2-diamino-benzene 
• 17966-68-6 N-benzoylaspartic acid 

Relevant articles and documents

Studies on Potential Antibacterial and Chelating Agents: Part I - Synthesis, Physicochemical Properties and Antibacterial Screening of Some Benzimidazoles

Six properly substituted benzimidazoles (I-VI) suitable for chelation have been synthesised from benzoylamino acids by condensation with o-phenylenediamine following Phillips and fusion methods.Dissociation constants of the benzoyl derivatives of glycine, (dl)-α-alanine, β-alanine, L-(-)-aspartic acid, L-(+)-glutamic acid and the six protonated benzamidobenzimidazoles (I-VI) in water-dioxane (1:1) at constant ionic strength (μ=0.5) at 20 deg C +/- 0.1 deg C have been determined by potentiometric titration.Structures of I-VI have been established on the basis of their elemental analysis, synthetic route, IR and PMR spectra and pK* values.Some of the compounds show significant antibacterial activity against gram + ve organisms only whereas corresponding sulphonamidobenzimidazoles are active against the gram - ve organism E. coli.