65707-74-6

Basic information

• Product Name: N-diphenylacetylglycine
• Synonyms: Glycine, N-(2,2-diphenylacetyl)-; Glycine, N-(diphenylacetyl)-; N-(Diphenylacetyl)glycine
• CAS NO: 65707-74-6
• Molecular Formula: C₁₆H₁₅NO₃
• Molecular Weight: 269.3
• Mol File: 65707-74-6.mol

Chemical Properties

• Boiling Point: 541.6°Cat760mmHg
• Flash Point: 281.4°C
• Appearance: /
• Density: 1.225g/cm³
• Vapor Pressure: 1.45E-12mmHg at 25°C
• Refractive Index: 1.595
• CAS DataBase Reference: N-diphenylacetylglycine(CAS DataBase Reference)
• NIST Chemistry Reference: N-diphenylacetylglycine(65707-74-6)
• EPA Substance Registry System: N-diphenylacetylglycine(65707-74-6)

Safety Data

• Hazardous Substances Data: 65707-74-6(Hazardous Substances Data)

Usage

Uses

Used in Coordination Chemistry:
N-diphenylacetylglycine is used as a ligand for forming stable and soluble complexes with metal ions. This property makes it useful in catalytic reactions and as a chelating agent, contributing to advancements in this scientific field.
Used in Organic Synthesis:
As a building block in organic synthesis, N-diphenylacetylglycine aids in the creation of various complex organic compounds, further expanding its utility in chemical research and development.
Used in Pharmaceutical Industry:
N-diphenylacetylglycine is utilized as a raw material in the synthesis of a range of pharmaceutical compounds, highlighting its importance in drug development and production.
Used in Biological Research:
N-diphenylacetylglycine has been studied for its potential biological activities such as anti-inflammatory and analgesic effects, indicating its possible use in the development of new therapeutic agents for treating inflammation and pain.

InChI:InChI=1/C16H15NO3/c18-14(19)11-17-16(20)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H,17,20)(H,18,19)

Upstream product

• 117-34-0 2,2-diphenylacetic acid 
• 753498-13-4 methyl 2-[(2,2-diphenylacetyl)amino]acetate 
• 1871-76-7 diphenylacetic acid chloride 
• 56-40-6 glycine 

Downstream Products

• 1579991-27-7 C₂₃H₁₉N₃O₂S 
• 1073179-08-4 C₆₀C₂H₃(C₅H₄N)NCH₂CH₂OCH₂CH₂OCH₂CH₂NHCOCH₂NHCOCH(C₆H₅)2 
• 137074-61-4 1-(N-(diphenylacetyl)aminoacetyl)-4-(pyridin-4-ylcyanomethyl)piperazine 
• 753498-15-6 3-(tert-butyl-dimethyl-silanyloxy)-2-(2-diphenylacetylamino-acetylamino)-propionic acid methyl ester 
• 753498-17-8 N-{[2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxymethyl-ethylcarbamoyl]-methyl}-2,2-diphenyl-acetamide 
• 1416547-73-3 C₄₇H₅₂N₂O₄ 

Relevant articles and documents

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Sew simple: How can you put a molecular bead on a thread when no recognition elements exist between them? A mechanically interlocking auxiliary assembles the macrocycle around a template, controlled submolecular translation moves the ring over the desired

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Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially.

Composition containing a penem or carbapenem antibiotic

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