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Benzothiazole, 2-[[(3,4-dichlorophenyl)methyl]sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76151-65-0

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76151-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76151-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,5 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76151-65:
(7*7)+(6*6)+(5*1)+(4*5)+(3*1)+(2*6)+(1*5)=130
130 % 10 = 0
So 76151-65-0 is a valid CAS Registry Number.

76151-65-0SDS

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-[(3,4-dichlorophenyl)methylsulfonyl]-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names -

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:76151-65-0 SDS

76151-65-0Downstream Products

76151-65-0Relevant academic research and scientific papers

Novel aromatic fluoroolefins via fluoro-Julia-Kocienski olefination

Allendoerfer, Nadine,Es-Sayed, Mazen,Nieger, Martin,Braese, Stefan

experimental part, p. 3439 - 3448 (2010/12/19)

Fluoroolefins, which play an increasingly important role as peptide mimics in pharmaceuticals and as crop protection agents, are generated using a fluoro-Julia-Kocienski olefination. Their preparation can easily be accomplished using a Mitsunobu reaction and subsequent oxidation to generate the required benzothiazolyl sulfones. The key step of this process was the electrophilic -fluorination of the sulfone with N-fluorobenzenesulfonimide. The last stage of the successful synthesis of the fluoroolefins was the modified Julia-Kocienski olefination under basic conditions. Further functionalization was followed with the application of a Suzuki reaction. Georg Thieme Verlag Stuttgart.

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