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89565-18-4

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89565-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89565-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89565-18:
(7*8)+(6*9)+(5*5)+(4*6)+(3*5)+(2*1)+(1*8)=184
184 % 10 = 4
So 89565-18-4 is a valid CAS Registry Number.

89565-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N-[4-(dimethylsulfamoyl)phenyl]benzamide

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:89565-18-4 SDS

89565-18-4Downstream Products

89565-18-4Relevant articles and documents

Some Novel Sulfanilyl Derivatives

Cremlyn, R. J.,Swinbourne, F. S.,Batchelor, A.,Honeyman, R.,Nash, D.,et al.

, p. 1029 - 1043 (2007/10/02)

Benzoic acid anilide and p-chloro, m-nitro, together with the 2,4-, 2,5- and 3,4-dichloro derivatives, react with chlorosulfonic acid in 1:4 molar ratios to give the corresponding sulfanilyl chlorides.However, nicotinic acid and isonicotinic acid anilides react with chlorosulfonic acid in 1:6 molar ratios only for conversion into the sulfanilyl chlorides. 2,4-Dichlorophenoxyacetic acid anilide reacts with chlorosulfonic acid in 1:3 molar ratio to give the sulfanilyl chloride; this reaction when carried out in 1:7 molar ratios of the reactants affords the disulfonylchloride.The various sulfanilyl chlorides are reacted with amines, azide ion, and hydrazine to give a range of sulfonyl compounds.The compounds prepared have been subjected to preliminary biological screening.

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