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Benzenepentanesulfonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62607-65-2

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62607-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62607-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62607-65:
(7*6)+(6*2)+(5*6)+(4*0)+(3*7)+(2*6)+(1*5)=122
122 % 10 = 2
So 62607-65-2 is a valid CAS Registry Number.

62607-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylpentane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names Benzenepentanesulfonic acid

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:62607-65-2 SDS

62607-65-2Relevant academic research and scientific papers

Sustainable access to sulfonic acids from halides and thiourea dioxide with air

Zhang, Hui,Wang, Ming,Jiang, Xuefeng

supporting information, p. 8238 - 8242 (2020/12/29)

A sustainable and mild one-step strategy is explored for the synthesis of aryl and alkyl sulfonic acids using a facile combination of halides and sulfur dioxide surrogates under air. The cheap industrial material thiourea dioxide was employed as an eco-friendly and easy-handling sulfur dioxide surrogate, while air was used as a green oxidant. Both aryl and alkyl sulfonic acids were obtained under transition metal-catalyzed or transition metal-free conditions. Mechanistic studies demonstrated that sulfinate was involved as an intermediate in this transformation. Notably, this protocol has been applied to the late-stage sulfonation of the drugs naproxen, isoxepac and ibuprofen.

COMPOUNDS AND METHODS FOR CONTROLLING BACTERIAL VIRULENCE

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Page 28, (2010/02/04)

Novel sulfonated homoserine lactones formula I have been found to act ac quorum sensing inhibitors. As such, they may be useful in the treatment of bacterial infections.

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