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2-[methyl(phenyl)amino]acetohydrazide (non-preferred name) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71480-85-8

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71480-85-8 Usage

Molecular weight

164.21 g/mol

Derivative of

Acetohydrazide

Functional groups

Methylphenylamino group attached to the acetyl group

Common uses

Synthesis of pharmaceutical and agrochemical products, research and development

Biological activities

Various biological activities

Potential applications

Medicine, agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 71480-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,8 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71480-85:
(7*7)+(6*1)+(5*4)+(4*8)+(3*0)+(2*8)+(1*5)=128
128 % 10 = 8
So 71480-85-8 is a valid CAS Registry Number.

71480-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(N-methylanilino)acetohydrazide

1.2 Other means of identification

Product number -
Other names N-methyl-N-phenylaminoacetichydrazide

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:71480-85-8 SDS

71480-85-8Relevant academic research and scientific papers

KINASE INHIBITOR

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Paragraph 0221; 0223, (2021/04/16)

The present invention aims to provide a novel kinase inhibitor and the like, and a therapeutic agent for a disease, a drug discovery screening method and the like utilizing such inhibitor and the like. The compound represented by the following formula (I) and a salt thereof can inhibit plural kinases including LATS (particularly LATS2) which is the major kinase in the Hippo signal transduction pathway. In addition, diseases or tissue damage associated with failure of cellular proliferation can be treated. Therefore, the present invention is beneficial, for example, in the research field of cell functions and diseases, in which the Hippo signal transduction pathway is involved, and the like. Furthermore, it is beneficial in the medical field for the treatment of such diseases and the like. wherein each symbol is as defined in the DESCRIPTION.

ADDITIVE COMPOSITION FOR CULTURE MEDIUM, ADDITIVE COMPOUND FOR CULTURE MEDIUM, AND METHOD FOR CULTURE OF CELLS OR TISSUE USING SAME

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Paragraph 0211; 0213, (2020/06/15)

The present invention provides a medium additive composition containing a compound represented by the following formula (I), or a salt thereof: {wherein each symbol is as defined in the DESCRIPTION.}

Synthesis of 2-[N-methyl-N-(4-iodo-phenyl)aminomethyl]-1,3,4-oxa- diazole and its use as a protective synthon for indirect iodination of ketosteroids

Shabsoug, Barakat M.,Hassan, Mohamad A.

, p. 96 - 98 (2007/10/03)

2-(N-methyl-N-phenylaminomethyl)-1, 3, 4 oxadiazole can readily be iodinated to 2-[N-methy-N-(4 -iodophenyl) aminomethyl] - 1, 3, 4-oxadiazole which in a one-step hydrolysis condensation serves as an indirect prosthetic moiety for iodination / radioiodina

Synthesis, spectral studies and biological activities of some N-bridged heterocycles derived from 3-arylaminomethyl-4-amino-5-mercapto-1,2,4- triazoles

Holla,Udupa

, p. 305 - 318 (2007/10/02)

Synthesis of four 3-arylaminomethyl-4-amino-5-mercapto-1,2,4-triazoles starting from substituted anilines is described. These triazoles were employed in the synthesis of some N-bridged heterocycles carrying arylaminomethyl substituents. All the newly synthesized compounds were characterized by analytical, NMR and mass spectral studies. Some of the newly synthesized compounds were screened for their antibacterial and antiviral properties.

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