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89805-98-1

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89805-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89805-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89805-98:
(7*8)+(6*9)+(5*8)+(4*0)+(3*5)+(2*9)+(1*8)=191
191 % 10 = 1
So 89805-98-1 is a valid CAS Registry Number.

89805-98-1SDS

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-but-2-enylsulfanyl-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-But-2t-enylmercapto-benzothiazol

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:89805-98-1 SDS

89805-98-1Downstream Products

89805-98-1Relevant articles and documents

The first stereoselective total synthesis of the immunosuppressive decalin derivative monascusic acid B 1

Kumar, Jayprakash Narayan,Das, Biswanath

, p. 863 - 865 (2014/04/17)

The first stereoselective total synthesis of the immunosuppressive decalin derivative monascusic acid B has been accomplished from (R)-(+)-pulegone involving Horner-Wadsworth-Emmons and Julia-Kocienski olefination reactions and Lewis acid catalyzed intramolecular Diels-Alder cyclization. Georg Thieme Verlag Stuttgart New York.

Selectivity in Allylic Substitution with Organometallics through Neighbouring Co-ordination. Part 2. Reactions of 2-Allylthiobenzothiazoles with Organocopper Reagents

Calo, Vincenzo,Lopez Luigi,Carlucci, Walter

, p. 2953 - 2956 (2007/10/02)

Efficient control of the regioselectivity in allylic substitutions with Grignard reagents in the presence of copper(I) bromide has been achieved by using 2-allylthiobenzothiazoles as electriphiles.The SN2:SN2' product ratio depends on the degree of co-ordination between the allylic reagent and the organometalic species.

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