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3,5-Pyridinedicarbothioic acid, 1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)-, S,S-diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81635-64-5

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81635-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81635-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,3 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81635-64:
(7*8)+(6*1)+(5*6)+(4*3)+(3*5)+(2*6)+(1*4)=135
135 % 10 = 5
So 81635-64-5 is a valid CAS Registry Number.

81635-64-5SDS

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 OSI-4164

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-4-(4-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarbothioic acid di-S-ethyl ester

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:81635-64-5 SDS

81635-64-5Relevant academic research and scientific papers

Esters of 1,4-dihydropyridine-3- and -3,5-carbothiolic acids

Vigante,Ozols,Dubur,Beilis,Belash,Prezhdo

, p. 170 - 178 (2007/10/02)

Methods for the preparation of esters of 1,4-dihydropyridine-3- and -3,5-carbothiolic acids were developed, and their structure and reactivity were studied. A comparative analysis was made of the spectroscopic characteristics of sulfur-containing esters of the 1,4-dihydropyridine series and their oxygen analogs. More strongly expressed electron-acceptor properties of the COSAlk groupings as compared with alkoxycarbonyl substituents were observed.

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