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BENZENEMETHANESULFONYL CHLORIDE, 3-METHOXY- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

163295-76-9

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163295-76-9 Usage

Chemical compound

Benzeneethanesulfonyl chloride, 3-methoxy-

Class

Aromatic sulfonyl chlorides

Uses

Reagent in the synthesis of pharmaceuticals and agrochemicals, sulfonating agent, intermediate in the production of various organic compounds

Effects

Corrosive, may cause skin, eyes, and respiratory irritation

Safety

Handle with caution, take proper safety precautions to minimize risk of exposure and harm

Check Digit Verification of cas no

The CAS Registry Mumber 163295-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,2,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163295-76:
(8*1)+(7*6)+(6*3)+(5*2)+(4*9)+(3*5)+(2*7)+(1*6)=149
149 % 10 = 9
So 163295-76-9 is a valid CAS Registry Number.

163295-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methoxyphenyl)methanesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 3-methoxybenzylsulfonyl chloride

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:163295-76-9 SDS

163295-76-9Relevant academic research and scientific papers

Asymmetric synthesis of α- and α,β-substituted β-alkoxycarbonyl sulfonates

Enders, Dieter,Adelbrecht, Jean-Claude,Harnying, Wacharee

, p. 2962 - 2968 (2007/10/03)

An efficient asymmetric synthesis of substituted β-alkoxycarbonyl sulfonates is described. Enantiopure α-substituted β-alkoxycarbonyl sulfonates can be obtained via α-alkylation of metalated sulfonates bearing 1,2:5,6-di-O-isopropylidene-α-D-allofuranose

Process for making an aldehyde

-

Page 20; 22, (2008/06/13)

A process for making an aromatic aldehyde in which a sulfoxide is reacted with a dihalogenated aromatic compound in the absence of an effective amount of an activating reagent. The aldehyde may then be used to make other compounds, such as a compound that acts as a cPLA inhibitor.

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