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115755-82-3

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115755-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115755-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,5 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115755-82:
(8*1)+(7*1)+(6*5)+(5*7)+(4*5)+(3*5)+(2*8)+(1*2)=133
133 % 10 = 3
So 115755-82-3 is a valid CAS Registry Number.

115755-82-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name CIS-1,2-DICYANO-1,2-BIS(2,4,5-TRIMETHYL-3-THIENYL)ETHENE

1.2 Other means of identification

Product number -
Other names cis-1,2-Cyclopropandiammoniumchlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:115755-82-3 SDS

115755-82-3Downstream Products

115755-82-3Relevant articles and documents

Thermally Irreversible Photochromic Systems. Reversible Photocyclization of Non-Symmetric Diarylethene Derivatives

Nakayama, Yasuhide,Hayashi, Koichiro,Irie, Masahiro

, p. 789 - 795 (2007/10/02)

Non-symmetric diarylethenes with an indole ring on one end and a thiophene, a benzothiophene, or a pyrrole ring on the other end of the double bond were synthesized in an attempt to get thermally irreversible photochromic compounds having absorption bands at longer wavelengths. 2-(1,2-Dimethyl-3-indolyl)-3-(2,4,5-trimethyl-3-thienyl)maleic anhydride (8a) underwent photoinduced cyclization/ring-opening reactions with relatively high quantum yields (cyclization quantum yield: 0.15; ring-opening quantum yield: 0.40), and the both isomers were thermally stable.The closed-ring form had the absorption maximum at 595 nm with the edge extending to 760 nm.Cyclization/ring-opening reactions of 8a and 2-(1,2-dimethyl-3-indolyl)-3-(2-methyl-3-benzothienyl)maleic anhydride (9a) were induced by Ar ion (488 nm) and He-Ne (633 nm) lasers.

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