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88701-65-9

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88701-65-9 Usage

Derivative of piperazine

Yes

Potential applications

Building block in the synthesis of pharmaceuticals and agrochemicals

Investigated properties

Anti-inflammatory and anti-tubercular

Safety concerns

Toxicity and potential hazards to human health and the environment due to hydrazide functional group

Further research needed

Yes, to understand potential uses and risks

Check Digit Verification of cas no

The CAS Registry Mumber 88701-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,0 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88701-65:
(7*8)+(6*8)+(5*7)+(4*0)+(3*1)+(2*6)+(1*5)=159
159 % 10 = 9
So 88701-65-9 is a valid CAS Registry Number.

88701-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylpiperazine-1-carbohydrazide

1.2 Other means of identification

Product number -
Other names 1-Piperazinecarboxylicacid,4-methyl-,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:88701-65-9 SDS

88701-65-9Relevant articles and documents

Synthesis and anti-trypanosomal activity of novel 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives

Cerecetto, Hugo,Di Maio, Rossanna,Ibarruri, Gerardo,Seoane, Gustavo,Denicola, Ana,Peluffo, Gonzalo,Quijano, Celia,Paulino, Margot

, p. 89 - 94 (2007/10/03)

Several novel semicarbazones derivatives were prepared from 5-nitro-2-furaldehyde or 5-nitrothiophene-2-carboxaldehyde, and tested in vitro as potential anti-trypanosomal agents. The compounds were prepared in good to excellent yields in 2-3 steps from readily available starting materials. Some derivatives were found to be active against Trypanosoma cruzi with an activity similar to that of Nifurtimox.

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