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94135-73-6

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94135-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94135-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,3 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94135-73:
(7*9)+(6*4)+(5*1)+(4*3)+(3*5)+(2*7)+(1*3)=136
136 % 10 = 6
So 94135-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2S/c1-6(10-7(2)9)8-4-3-5-11-8/h3-6H,1-2H3

94135-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-thiophen-2-ylethyl acetate

1.2 Other means of identification

Product number -
Other names Essigsaeure-(2-[2]thienyl-aethylester)

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:94135-73-6 SDS

94135-73-6Relevant articles and documents

Supramolecular assembly of a quaterthiophene surfactant

Jiang, Lu,Hughes, Robert C.,Sasaki, Darryl Y.

, p. 1028 - 1029 (2004)

A newly synthesized oligothiophene surfactant self-assembles into unilamellar vesicles in aqueous solution and exhibits semiconductive behavior as a cast film.

Synthesis and class III type antiarrhythmic activity of 4-Aroyl (and Aryl)-1-aralkylpiperazines

Kanojia, Ramesh M.,Salata, Joseph J.,Kauffman, Jack

, p. 2819 - 2823 (2007/10/03)

The synthesis and in vitro Class III antiarrhythmic activity of several 4-aroyl (and aryl)-1-aralkylpiperazine and piperidine derivatives are described. Among several potent compounds identified in the series, RWJ-28810 (3), with its EC20 of 3 nM, ranks as one of the most potent (in vitro) compounds reported. (C) 2000 Elsevier Science Ltd.

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