Cas 1402748-84-8,((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene

1402748-84-8

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Basic information

Product Name: ((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene
Synonyms: ((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene
CAS NO:1402748-84-8
Molecular Formula:
Molecular Weight: 456.529
EINECS: N/A
Product Categories: N/A
Mol File: 1402748-84-8.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: ((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene(CAS DataBase Reference)
NIST Chemistry Reference: ((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene(1402748-84-8)
EPA Substance Registry System: ((1E,6E)-4-(phenylsulfonyl)-4-(trifluoromethyl)hepta-1,6-diene-1,7-diyl)dibenzene(1402748-84-8)

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: 1402748-84-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1402748-84-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,7,4 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1402748-84:
(9*1)+(8*4)+(7*0)+(6*2)+(5*7)+(4*4)+(3*8)+(2*8)+(1*4)=148
148 % 10 = 8
So 1402748-84-8 is a valid CAS Registry Number.

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1402748-84-8Relevant articles and documents

Palladium-catalyzed allylation of 2,2,2-trifluoroethyl phenyl sulfone, a potential 2,2,2-trifluoroethyl pronucleophile

Zhang, Wei,Zhao, Yanchuan,Ni, Chuanfa,Mathew, Thomas,Hu, Jinbo

, p. 6565 - 6568,4 (2012/12/12)

A palladium-catalyzed allylation reaction of PhSO2CH 2CF3 (2) with a variety of allyl carbonates has been successfully developed for selective 2,2,2-trifluoroethylation under neutral conditions. With this method, the 1-phe

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