16533-70-3

Basic information

• Product Name: N-(3,5-dinitrobenzoyl)glycine
• CAS NO: 16533-70-3
• Molecular Formula: C₉H₇N₃O₇
• Molecular Weight: 269.1678
• Mol File: 16533-70-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 514.2°C at 760 mmHg
• Flash Point: 264.8°C
• Density: 1.635g/cm³
• Vapor Pressure: 2.12E-11mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: N-(3,5-dinitrobenzoyl)glycine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,5-dinitrobenzoyl)glycine(16533-70-3)
• EPA Substance Registry System: N-(3,5-dinitrobenzoyl)glycine(16533-70-3)

Safety Data

• Hazardous Substances Data: 16533-70-3(Hazardous Substances Data)

Upstream product

• 65-85-0 benzoic acid 
• 99-34-3 3,5-dinitrobenzoic acid 
• 56-40-6 glycine 
• 99-33-2 3,5-dinitrobenoyl chloride 

Downstream Products

• 4212-00-4 2-(3,5-dinitro-phenyl)-4-thiophen-2-ylmethylene-4H-oxazol-5-one 
• 19646-42-5 3,3'-{4-[2-(3,5-dinitro-phenyl)-5-oxo-oxazol-4-ylidenemethyl]-phenylazanediyl}-bis-propionitrile 
• 20448-28-6 3,3'-{4-[2-(3,5-dinitro-phenyl)-5-oxo-oxazol-4-ylidenemethyl]-3-methyl-phenylazanediyl}-bis-propionitrile 
• 39052-69-2 4-[4-(benzyl-methyl-amino)-benzylidene]-2-(3,5-dinitro-phenyl)-4H-oxazol-5-one 
• 134269-10-6 DnBz-Gly-Phe-NH-c 
• 134269-06-0 DnBz-Gly-Phe-NH-Meq 
• 134269-02-6 DnBz-Gly-Phe-NH-Mec 
• 1037569-85-9 C₂₆H₂₂N₈O₁₂ 
• 1037570-01-6 C₃₀H₂₂N₈O₁₃ 
• 1281969-77-4 C₁₆H₇BrFN₃O₆ 
• 1335100-14-5 2-(2-(3,5-dinitrobenzamido)acetoxy)-N,N,N-trimethylethanaminium chloride 

Relevant articles and documents

Novel water-soluble red-emitting poly(p -phenylenevinylene) derivative: Synthesis, characterization, and fluorescent acetylcholinesterase assays

A new cyano-substituted poly(p-phenylenevinylene) (PPV) derivative, MEOPS-CNPPV, is synthesized through Knoevenagel condensation of anionic diacetonitrile and neutral dialdehyde and characterized by 1H NMR, IR, elemental analysis, and gel-permeation chromatography (GPC). To our knowledge, the polymer is the first water-soluble red-emitting PPV derivative. The absorption and emission wavelength of this water-soluble conjugated polymer (CP) depend on the solvent. In buffer solution, the fluorescence of MEOPS-CNPPV is quenched by cationic dinitrobenzene derivatives. Further research indicates that dinitrobenzene derivative with a more flexible structure exhibits a larger Ksv. Making use of the charge reversal of dinitrobenzene-modified substrate, a "turn-on" method is developed for AChE activity assay with the new polymer as a fluorophore. This convenient and direct fluorometric assay thus provides a platform for novel red-emitting sensory systems.

Synthesis, characterization and biological activity of Cu(II) chelates with some amino acid derivatives

The complexing behaviour of seventeen amino acid derivatives towards Cu(II) has been studied.Complexes of the types Cu(RH)*xH2O, Cu(RH).Cu(OH)2*xH2O and Cu(R'H)2*yH2O have been prepared and characterized by IR, ESR, electronic spectral, magnetic moment and analytical data.On the basis of differences and direction of the shifts in the IR frequencies of vas OCO and vs OCO modes and ESR spectra, bonding modes of carboxylate group have been established.Biological activitu of complexes is more than that of the free metal ion and the ligands.