Cas 402912-73-6,9-Anthracenecarboxamide, N-[4-[1-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]-

402912-73-6

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Basic information

Product Name: 9-Anthracenecarboxamide, N-[4-[1-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]-
Synonyms:
CAS NO:402912-73-6
Molecular Formula: C37H38N2O
Molecular Weight: 526.722
EINECS: N/A
Product Categories: N/A
Mol File: 402912-73-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 9-Anthracenecarboxamide, N-[4-[1-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 9-Anthracenecarboxamide, N-[4-[1-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]-(402912-73-6)
EPA Substance Registry System: 9-Anthracenecarboxamide, N-[4-[1-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]-(402912-73-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 402912-73-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 402912-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,9,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 402912-73:
(8*4)+(7*0)+(6*2)+(5*9)+(4*1)+(3*2)+(2*7)+(1*3)=116
116 % 10 = 6
So 402912-73-6 is a valid CAS Registry Number.

402912-73-6Upstream product

402912-73-6Downstream Products

402912-73-6Relevant articles and documents

A supramolecular system for quantifying aromatic stacking interactions

Adams, Harry,Hunter, Christopher A.,Lawson, Kevin R.,Perkins, Julie,Spey, Sharon E.,Urch, Christopher J.,Sanderson, John M.

, p. 4863 - 4877 (2007/10/03)

A supramolecular complex for investigating the thermodynamic properties of intermolecular aromatic stacking interactions has been developed. The conformation of the complex is locked in a single well-defined conformation by an array of H-bonding interacti

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