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2-BROMO-1-(5-CHLORO-2-METHYL-THIOPHEN-3-YL)-ETHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

528604-96-8

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528604-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 528604-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,6,0 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 528604-96:
(8*5)+(7*2)+(6*8)+(5*6)+(4*0)+(3*4)+(2*9)+(1*6)=168
168 % 10 = 8
So 528604-96-8 is a valid CAS Registry Number.

528604-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-chloro-3-(bromoacetyl)thiophene

1.2 Other means of identification

Product number -
Other names 5-chloro-2-methyl-3-(bromoacetyl)thiophene

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:528604-96-8 SDS

528604-96-8Upstream product

528604-96-8Relevant academic research and scientific papers

Study on photochromism of diarylethenes with a 2,5-dihydropyrrole bridging unit: A convenient preparation of 3,4-diarylpyrroles from 3,4-diaryl-2,5- dihydropyrroles

Chen, Yi,Zeng, De X.,Xie, Nan,Dang, Yi Z.

, p. 5001 - 5005 (2007/10/03)

Symmetric and nonsymmetric diarylethenes with a 2,5-dihydropyrrole bridging unit have been prepared, and the photochromic properties are investigated. Both symmetric and nonsymmetric diarylethenes with 2,5-dihydropyrrole bridging units undergo reversible ring-opening and ring-closing photoisomerization reactions in nonpolar solvents with UV/vis light, and some of them exhibit good fatigue resistance and no marked degradation detected after 10 cycles via an on/off switch. In polar solvents, however, photochromic diarylethenes with 2,5-dihydropyrrole bridging units produce 3,4-diarylpyrrole derivatives instead of the ring-closing isomer of diarylethenes with UV light irradiation. A class of N-substituted 3,4-diphenylethenes with 2,5-dihydropyrrole bridging units were prepared and used as templates to investigate the conversion reactions. The mechanism of photoconversion of 3,4-diaryl-2,5-dihydropyrroles to 3,4-diarylpyrroles was explored as well.

Synthesis and photochromic properties of functional diarylethene with a 2,5-dihydrothiophene bridging unit

Chen, Yi,Zeng, De X.,Fan, Mei G.

, p. 1435 - 1437 (2007/10/03)

(Matrix presented) A novel synthetic route to symmetric and nonsymmetric dithienylethene derivatives with a 2,5-dihydrothiophene bridging unit was described. A class of new functional photochromic compounds was prepared and showed photochromic properties similar to those of known diarylethenes.

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