Cas 1372715-06-4,1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene

1372715-06-4

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Basic information

Product Name: 1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene
Synonyms: 1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene
CAS NO:1372715-06-4
Molecular Formula:
Molecular Weight: 560.56
EINECS: N/A
Product Categories: N/A
Mol File: 1372715-06-4.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: 1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene(1372715-06-4)
EPA Substance Registry System: 1-(2-methylnaphth-1-yl)-2-[2-methyl-5-(4-(1,3-dioxolan-2-yl)phenyl)thien-3-yl]perfluorocyclopentene(1372715-06-4)

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: 1372715-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1372715-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,7,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1372715-06:
(9*1)+(8*3)+(7*7)+(6*2)+(5*7)+(4*1)+(3*5)+(2*0)+(1*6)=154
154 % 10 = 4
So 1372715-06-4 is a valid CAS Registry Number.

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1372715-06-4Relevant articles and documents

The effect of the formyl group position upon asymmetric isomeric diarylethenes bearing a naphthalene moiety

Wang, Renjie,Pu, Shouzhi,Liu, Gang,Cui, Shiqiang

, p. 1018 - 1026 (2012/08/28)

Three new isomeric asymmetric diarylethenes with a naphthyl moiety and a formyl group at the para, meta or ortho position of the terminal benzene ring were synthesized. Their photochromism, fluorescent-switch, and electrochemical properties were investiga

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