Cas 42549-14-4,1H-Inden-2-amine, N-(2,6-dimethylphenyl)-1-[(2,6-dimethylphenyl)imino]-3-phenyl-

42549-14-4

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Basic information

Product Name: 1H-Inden-2-amine, N-(2,6-dimethylphenyl)-1-[(2,6-dimethylphenyl)imino]-3-phenyl-
Synonyms:
CAS NO:42549-14-4
Molecular Formula: C31H28N2
Molecular Weight: 428.577
EINECS: N/A
Product Categories: N/A

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: 1H-Inden-2-amine, N-(2,6-dimethylphenyl)-1-[(2,6-dimethylphenyl)imino]-3-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Inden-2-amine, N-(2,6-dimethylphenyl)-1-[(2,6-dimethylphenyl)imino]-3-phenyl-(42549-14-4)
EPA Substance Registry System: 1H-Inden-2-amine, N-(2,6-dimethylphenyl)-1-[(2,6-dimethylphenyl)imino]-3-phenyl-(42549-14-4)

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: 42549-14-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 42549-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,4 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42549-14:
(7*4)+(6*2)+(5*5)+(4*4)+(3*9)+(2*1)+(1*4)=114
114 % 10 = 4
So 42549-14-4 is a valid CAS Registry Number.

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42549-14-4Relevant academic research and scientific papers

Cyclic meso-ionic heterocycles. Part 24. The reaction of 1,2-dithiolium-4-olates with aniline. The formationof 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine

Newton, Christopher G.,Ollis, W. David,Rowson, Graham P.,Hamor, Margaret J.,Hamor, Thomas A.

, p. 8127 - 8142 (2007/10/02)

Reaction of the type B meso-ionic heterocycle 3,5-diphenyl-1,2-dithiolium-4-olate (1) with aniline yields N-phenyl-(3-phenyl-1-phenylimino-inden-2-yl)-amine (10) and 11-phenylbenz[bindeno[2,1-e]-1,4-thiazine (12). Mechanistic investigations establish that

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