71764-61-9

Basic information

• Product Name: N,N'N-Trisphenyl-1,3,5-benzenetricarbonamide
• Synonyms: N,N'N-Trisphenyl-1,3,5-benzenetricarbonamide
• CAS NO: 71764-61-9
• Molecular Weight: 435.482
• Mol File: 71764-61-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N,N'N-Trisphenyl-1,3,5-benzenetricarbonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'N-Trisphenyl-1,3,5-benzenetricarbonamide(71764-61-9)
• EPA Substance Registry System: N,N'N-Trisphenyl-1,3,5-benzenetricarbonamide(71764-61-9)

Safety Data

• Hazardous Substances Data: 71764-61-9(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 4422-95-1 1,3,5-benzene tris(carbonyl chloride) 
• 554-95-0 benzene-1,3,5-tricarboxylic acid 
• 587-14-4 N,N'-diphenylsulfamide 

Downstream Products

• 117070-36-7 N,N',N-trimethyl-N,N',N-triphenyl-1,3,5-benzenetricarboxamide 

Relevant articles and documents

General method for quickly synthesizing bridge-linked bisamide, triamide and tetraamide derivatives through ultrasonic radiation method and application

The invention belongs to the technical field of organic synthesis, specifically discloses bridge-linked bisamide, triamide and tetraamide derivatives and a general method for ultrasonic radiation quick synthesis thereof, and also relates to the applicatio

Insights into the formation of chiral second sphere coordination complexes with aromatic tris amines: combined single crystal X-ray crystallography and molecular modeling analyses

A family of isostructural, chiral supramolecular networks have been obtained in the solid state by exploiting second sphere coordination interactions in the self-assembly of achiral tris amines L1 and L2 with tetrahalometallate and halide ions. Quantum-Mechanical (QM) calculations specific for solid phases provided additional insights into the intramolecular and packing interactions which determine chirality, pointing to a direct effect of the methyl groups of the central benzene ring.

Discovery of small molecule CXCR4 antagonists

In light of a proposed molecular mechanism for the C-X-C chemokine receptor type 4 (CXCR4) antagonist 1 (AMD3100), a template with the general structure 2 was designed, and 15 was identified as a lead by means of an affinity binding assay against the liga