Cas 169173-75-5,1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene

169173-75-5

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Basic information

Product Name: 1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene
Synonyms: 1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene
CAS NO:169173-75-5
Molecular Formula:
Molecular Weight: 776.991
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: 1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene(169173-75-5)
EPA Substance Registry System: 1,2-Bis-<5'-(3'',5''-di-tert-butyl-4''-hydroxyphenyl)-2'-methylthien-3'-yl>perfluorocyclopentene(169173-75-5)

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: 169173-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169173-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,1,7 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169173-75:
(8*1)+(7*6)+(6*9)+(5*1)+(4*7)+(3*3)+(2*7)+(1*5)=165
165 % 10 = 5
So 169173-75-5 is a valid CAS Registry Number.

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169173-75-5Relevant academic research and scientific papers

A Dual-Mode Molecular Switching Device: Bisphenolic Diarylethenes with Integrated Photochromic and Electrochromic Properties

Kawai, Stephen H.,Gilat Sylvain L.,Ponsinet, Rachel,Lehn, Jean-Marie

, p. 285 - 293 (2007/10/02)

The bisphenolic dithienylethene molecules 1a and 1b were synthesized in overall yields of 45percent from 4-bromoanisole and 44percent from 2,6-di-tert-butyl-4-iodophenol, respectively.The corresponding extended quinones 3a and 3b were also prepared.Photoc

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