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69212-33-5

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69212-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69212-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69212-33:
(7*6)+(6*9)+(5*2)+(4*1)+(3*2)+(2*3)+(1*3)=125
125 % 10 = 5
So 69212-33-5 is a valid CAS Registry Number.

69212-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-3-[(2-chloropyridin-3-yl)disulfanyl]pyridine

1.2 Other means of identification

Product number -
Other names 2,2'-dichloro-3,3'-disulfanediyl-bis-pyridine

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:69212-33-5 SDS

69212-33-5Upstream product

69212-33-5Downstream Products

69212-33-5Relevant articles and documents

Aqueous process chemistry: The preparation of aryl sulfonyl chlorides

Hogan, Philip J.,Cox, Brian G.

scheme or table, p. 875 - 879 (2010/04/22)

The use of aqueous acidic conditions for the preparation of arylsulfonyl chlorides from diazonium salts in the presence of copper salts, preferably CuCl, together with thionyl chloride as the sulfur dioxide source, has considerable advantages over recommended literature procedures, whereby reactions are carried out in acetic acid with minimisation of water content of the solvent. The method has been shown to be successful for a wide range of electron-deficient and electron-neutral aryl substrates. The sulfonyl chlorides are protected from hydrolysis by their low solubility in water, which results in their direct precipitation from the reaction mixture in good yields (>70%) and high strength (>98% w/w). The aqueous process, which is additionally safer and more robust, can be readily scaled up and has significant environmental benefits.

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