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74752-56-0

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74752-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74752-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,5 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74752-56:
(7*7)+(6*4)+(5*7)+(4*5)+(3*2)+(2*5)+(1*6)=150
150 % 10 = 0
So 74752-56-0 is a valid CAS Registry Number.

74752-56-0SDS

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 methyl N-methyl-N-[(E)-pyridin-2-ylmethylideneamino]carbamodithioate

1.2 Other means of identification

Product number -
Other names methyl 3-<(2-pyridyl)-methylene>methylhydrazinecarbodithioate

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:74752-56-0 SDS

74752-56-0Downstream Products

74752-56-0Relevant articles and documents

Unusually Facile Ring-Opening Reaction in the Pyridine System

Scovill, John P.,Silverton, J.V.

, p. 4372 - 4376 (2007/10/02)

Reaction of 2-acetylpyridine with methyl 1-methylhydrazinecarbodithioate (2) resulted in formation of methyl (E,Z,E)-methylhydrazinecarbodithioate (4b) rather than the expected hydrazone, 3b.Reaction of pyridine-2-carboxaldehyde with 2, however, gave mostly the corresponding hydrazone 3a and some triazine 4a.Alkylation of 4a and 4b with iodomethane afforded the 3-methylthio derivatives 8a and 8b, respectively.The structure of 8a was determined by 1H NMR spectrometry and confirmed by a single-crystal X-ray analysis.Reaction of hydrazone 3b with 2 gave 4b, while treatment of 3b with dimethylamine afforded 6-(dimethylamino)-3,6-dihydro-1,3-dimethyl-4H-pyrido-triazine-4-thione (14a).Alkylation of 14a with iodomethane in aqueous base resulted in the formation of (Z,E)-4--2-butenal (15).Reaction of aldehyde 15 with 2 gave 4b.

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