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52776-76-8

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52776-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52776-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52776-76:
(7*5)+(6*2)+(5*7)+(4*7)+(3*6)+(2*7)+(1*6)=148
148 % 10 = 8
So 52776-76-8 is a valid CAS Registry Number.

52776-76-8SDS

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 4-methyl-N-pyridin-2-ylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4-methyl-N-(pyridin-2-yl)benzenesulfonamide

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:52776-76-8 SDS

52776-76-8Relevant articles and documents

Chemoselective Cleavage of Acylsulfonamides and Sulfonamides by Aluminum Halides

Sang, Dayong,Dong, Bingqian,Liu, Yunfeng,Tian, Juan

, p. 3586 - 3595 (2022/02/25)

The chemoselective cleavage of C-N bonds of amides, sulfonamides, and acylsulfonamides by aluminum halides is described. AlCl3and AlI3display complementary reactivities toward N-alkyl and N-acyl moieties. N-Alkylacylsulfonamides, sec

A multifunctional reagent designed for the site-selective amination of pyridines

Fier, Patrick S.,Kim, Suhong,Cohen, Ryan D.

, p. 8614 - 8618 (2020/06/05)

We report the development of a multifunctional reagent for the direct conversion of pyridines to Boc-protected 2-aminopyridines with exquisite site selectivity and chemoselectivity. The novel reagent was prepared on 200-g scale in a single step, reacts in the title reaction under mild conditions without precautions toward air or moisture, and is tolerant of nearly all common functionality. Experimental and in situ spectroscopic monitoring techniques provide detailed insights and unexpected findings for the unique reaction mechanism.

TRPC5 INHIBITORS AND METHODS OF USING SAME

-

Paragraph 00128; 00134, (2019/04/10)

Provided herein are TRPC5 inhibitors and methods of using the same, e.g., to protect podocytes and/or treat kidney disease.

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