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3-AMINO-4-METHYLBENZENECARBOHYDRAZIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

845884-82-4

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845884-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 845884-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 845884-82:
(8*8)+(7*4)+(6*5)+(5*8)+(4*8)+(3*4)+(2*8)+(1*2)=224
224 % 10 = 4
So 845884-82-4 is a valid CAS Registry Number.

845884-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-methylbenzohydrazide

1.2 Other means of identification

Product number -
Other names 3-amino-4-methyl-benzoic acid hydrazide

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:845884-82-4 SDS

845884-82-4Downstream Products

845884-82-4Relevant academic research and scientific papers

Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides

Rando, Daniela G.,Avery, Mitchell A.,Tekwani, Babu L.,Khan, Shabana I.,Ferreira, Elizabeth I.

, p. 6724 - 6731 (2008/12/22)

A series of 53 nitro derivatives rationally designed were obtained by parallel synthesis and screened against Leishmania donovani. Six compounds exhibited IC50 values lower than standard drugs. Brief SAR analysis revealed that substitution is important to the activity. Nitrothiophene analogues were more potent than the nitrofuran ones. This was attributed to the ability of sulfur atoms in accommodating electrons from nitro group, which facilitate its reduction and therefore the formation of free radicals lethal to parasites.

Heteroaryl-substituted pyrrolo-triazine compounds useful as kinase inhibitors

-

, (2008/06/13)

Compounds having the formula (I), and pharmaceutically acceptable salts, prodrugs, and solvates thereof, are useful as kinase inhibitors, wherein R1, R2, R3, R4, R5, R6, X and Z are as described in the specification.

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