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77484-08-3

77484-08-3

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77484-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77484-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77484-08:
(7*7)+(6*7)+(5*4)+(4*8)+(3*4)+(2*0)+(1*8)=163
163 % 10 = 3
So 77484-08-3 is a valid CAS Registry Number.

77484-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methyl-4-nitrophenyl)hydrazine

1.2 Other means of identification

Product number -
Other names 5-Nitro-2-hydrazino-toluol

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:77484-08-3 SDS

77484-08-3Upstream product

77484-08-3Downstream Products

77484-08-3Relevant articles and documents

A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones

Miles, Dillon H.,Guasch, Joan,Toste, F. Dean

supporting information, p. 7632 - 7635 (2015/07/02)

The enantioselective addition of anilines to azoalkenes was accomplished through the use of a chiral phosphoric acid catalyst. The resulting α-arylamino hydrazones were obtained in good yields and excellent enantioselectivities and provide access to enantioenriched α-arylamino ketones. A serendipitous kinetic resolution of racemic α-arylamino hydrazones is also described.

Antithrombotic carboxylic acid amides

-

, (2008/06/13)

Carboxylic acid amides of formula having antithrombotic activity and a factor Xa-inhibiting activity. Exemplary are: 2-(5-amidino-2-hydroxy-phenyl)-N-[3-methyl-4-(2-tert-butoxycarbonylaminomethyl -benzimidazol-1-yl)-phenyl]-acetamide; 2-(5-amidino-2-hydro

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