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51304-72-4

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51304-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51304-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,0 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51304-72:
(7*5)+(6*1)+(5*3)+(4*0)+(3*4)+(2*7)+(1*2)=84
84 % 10 = 4
So 51304-72-4 is a valid CAS Registry Number.

51304-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Methylsulfanyl-phenyl)-hydrazine

1.2 Other means of identification

Product number -
Other names 3-methylthiophenylhydrazine

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:51304-72-4 SDS

51304-72-4Relevant articles and documents

Palladium-catalyzed cross-coupling of aryl chlorides and tosylates with hydrazine

Lundgren, Rylan J.,Stradiotto, Mark

supporting information; experimental part, p. 8686 - 8690 (2011/01/08)

Hydrazine is not a problem anymore: The title transformation is the first reaction to yield aryl hydrazines through the cross-coupling of aryl chlorides and tosylates with hydrazine. An appropriately designed palladium catalyst allows this reaction to proceed rapidly under mild conditions, and with excellent chemoselectivity (see scheme; Ad=adamantyl, Ts=4-toluenesulfonyl).

Carbazole methyl malonates

-

, (2008/06/13)

A process for the preparation of α-methyl-carbazole-2-acetic acids, which comprises reacting an α-methyl-3-oxocyclohexane malonic acid di-lower alkyl ester with a substituted phenylhydrazine, and thereafter sequentially oxidizing and hydrolyzing the reaction product to obtain the desired acid, is described.

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