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Benzothiazole, 6-tert-butyl-2-methyl- (7CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91642-74-9

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91642-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91642-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,4 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91642-74:
(7*9)+(6*1)+(5*6)+(4*4)+(3*2)+(2*7)+(1*4)=139
139 % 10 = 9
So 91642-74-9 is a valid CAS Registry Number.

91642-74-9SDS

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 6-tert-butyl-2-methyl-benzothiazole

1.2 Other means of identification

Product number -
Other names 6-tert-Butyl-2-methyl-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:91642-74-9 SDS

91642-74-9Downstream Products

91642-74-9Relevant academic research and scientific papers

Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles

Franzmann, Peter,Beil, Sebastian B.,Schollmeyer, Dieter,Waldvogel, Siegfried R.

, p. 1936 - 1940 (2019/01/14)

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5-mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

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