Cas 1425513-34-3,2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene

1425513-34-3

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Basic information

Product Name: 2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene
Synonyms: 2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene
CAS NO:1425513-34-3
Molecular Formula:
Molecular Weight: 646.675
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: 2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene(CAS DataBase Reference)
NIST Chemistry Reference: 2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene(1425513-34-3)
EPA Substance Registry System: 2,3-diphenyl-6-(phenyl(4-(trifluoromethyl)phenyl)methyl)-1-(4-(trifluoromethyl)phenyl)-1H-indene(1425513-34-3)

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: 1425513-34-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1425513-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,5,5,1 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1425513-34:
(9*1)+(8*4)+(7*2)+(6*5)+(5*5)+(4*1)+(3*3)+(2*3)+(1*4)=133
133 % 10 = 3
So 1425513-34-3 is a valid CAS Registry Number.

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1425513-34-3Relevant academic research and scientific papers

Synthesis of multisubstituted indenes via iron-catalyzed domino reaction of benzylic compounds and alkynes

Chen, Yongxin,Li, Kangning,Liu, Xiang,Zhu, Jiaoyan,Chen, Baohua

supporting information, p. 130 - 134 (2013/02/25)

A novel approach to synthesizing multisubstituted indenes by iron-catalyzed domino reaction of benzylic compounds and alkynes under mild conditions was developed. This system could be applied to various available substrates in a one-step synthetic procedure in moderate to good yields. Georg Thieme Verlag Stuttgart · New York.

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