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111480-84-3

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111480-84-3 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 111480-84-3 differently. You can refer to the following data:
1. 2-Pyridinesulfonyl Chloride Hydrochloride is a useful reactant for the preparation of benzamides as 11β-hydroxysteroid dehydrogenase type 1 modulators for the treatment of metabolic syndromes.
2. 2-Chlorosulfonyl-pyridinium chloride is used for preparation of piperidine derivatives as tachykinin receptor antagonists.

Check Digit Verification of cas no

The CAS Registry Mumber 111480-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111480-84:
(8*1)+(7*1)+(6*1)+(5*4)+(4*8)+(3*0)+(2*8)+(1*4)=93
93 % 10 = 3
So 111480-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H4ClNO2S.ClH/c6-10(8,9)5-3-1-2-4-7-5;/h1-4H;1H

111480-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridine-2-sulfonyl chloride,hydrochloride

1.2 Other means of identification

Product number -
Other names Pyridine-2-sulfonyl chloride hydrochloride

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:111480-84-3 SDS

111480-84-3Upstream product

111480-84-3Relevant articles and documents

NaClO2-mediated preparation of pyridine-2-sulfonyl chlorides and synthesis of chiral sulfonamides

Xu, Dong,Yang, Shiyi,Gao, Aijun,Yang, Zhanhui

, p. 463 - 473 (2020/07/03)

A simple method to prepare azaarenesulfonyl chlorides by NaClO2-mediated oxidative chlorination of azaarenethiols have been developed, with water as the solvent. Easy purification by simple extraction and concentration gives the products in good yields. The azaarenesulfonyl chlorides readily undergo condensation with chiral amines to afford chiral sulfonamides.

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