347165-20-2

Basic information

• Product Name: 1,3,5-benzenetricarbonyl triazide
• Synonyms: 1,3,5-benzenetricarbonyl triazide
• CAS NO: 347165-20-2
• Molecular Weight: 285.181
• Mol File: 347165-20-2.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 1,3,5-benzenetricarbonyl triazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-benzenetricarbonyl triazide(347165-20-2)
• EPA Substance Registry System: 1,3,5-benzenetricarbonyl triazide(347165-20-2)

Safety Data

• Hazardous Substances Data: 347165-20-2(Hazardous Substances Data)

Upstream product

• 4422-95-1 1,3,5-benzene tris(carbonyl chloride) 
• 36997-31-6 benzene-1,3,5-tricarboxylic acid trihydrazide 
• 554-95-0 benzene-1,3,5-tricarboxylic acid 
• 4105-92-4 triethyl benzene-1,3,5-tricarboxylate 

Downstream Products

• 7373-27-5 1,3,5-benzenetriisocyanate 

Relevant articles and documents

Synthesis, crystal structure and gas uptake properties of a urea-functionalized rht-type metal-organic framework

A hexatopic C3-symmetrical 5,5′,5″-(((benzene-1,3,5-triyltris(azanediyl))tris(carbonyl))tris-(azanediyl))triisophthalic acid (H6-1) linker containing tri-urea groups has been designed and synthesized through the reaction between 1,3,

Tricarbamate of 1,3,5-triaminobenzene via Curtius rearrangement of trimesic acid and subsequent nitration

The triethyl tricarbamate of 1,3,5-triaminobenzene was prepared from trimesic acid in five steps with 70% overall yield. The tricarbamate underwent nitration to give the mono-, di-, or trinitro analogs in excellent yield. Copyright Taylor & Francis Group, LLC.

Low molecular weight organogelators derived from threefold symmetric tricarbamates

A group of new low molecular weight organogelators based on threefold symmetric tricarbamate were synthesized and characterized. The tricarbamates with long alkyl chains were able to gelate a wide range of polar and nonpolar organic solvents such as aceto

Preferred Binding of Carboxylates by Chiral Urea Derivatives Containing α-Phenylethyl Group

An efficient, simple protocol for the synthesis of a new family of chiral ureas 1 – 4 is described. The binding properties of 1 – 4 toward different anion (acetate, benzoate, fluoride, and chloride) have been studied by1H-NMR titration and have been observed in the case of 4 is a selective receptor for acetate. The theoretical calculation M06/6-311+G(d,p) helped us explain the binding properties observed. The most interesting observation is that this calculated structure is consistent with expected, based on the concept of allylic 1,3-strain (A1,3strain). When chiral caboxylates were studied, urea 1 was the best in discriminating between enantiomers.