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N-(3-aminophenyl)-N-methylacetamide is a chemical compound with the chemical formula C10H13N2O. It is a derivative of acetamide, featuring a methyl group and an aminophenyl group attached to the nitrogen atom. N-(3-aminophenyl)-N-methylacetamide is recognized for its potential in medicinal chemistry and drug development due to its versatile pharmacological properties.

61679-27-4

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61679-27-4 Usage

Uses

Used in Pharmaceutical Synthesis:
N-(3-aminophenyl)-N-methylacetamide is utilized as a building block in organic synthesis for the preparation of various pharmaceuticals and biologically active compounds. Its structural features make it a valuable component in the creation of new drugs with potential therapeutic benefits.
Used in Anti-inflammatory Applications:
In the medical field, N-(3-aminophenyl)-N-methylacetamide is used as an anti-inflammatory agent, helping to reduce inflammation which is a common symptom in various diseases and conditions.
Used as an Analgesic:
N-(3-aminophenyl)-N-methylacetamide also serves as an analgesic, providing pain relief, which is crucial in managing acute and chronic pain scenarios.
Used as an Antipyretic Agent:
N-(3-aminophenyl)-N-methylacetamide is used to reduce fever, making it a potential candidate for treating conditions characterized by elevated body temperature.
Used in Neurodegenerative Disorder Treatment:
It has been investigated for its potential role in the treatment of neurodegenerative disorders, suggesting that it may have properties that could slow disease progression or alleviate symptoms.
Used in Cancer Treatment Research:
Furthermore, N-(3-aminophenyl)-N-methylacetamide has been studied for its potential use in cancer treatment, indicating that it may contribute to therapeutic strategies against various types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 61679-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61679-27:
(7*6)+(6*1)+(5*6)+(4*7)+(3*9)+(2*2)+(1*7)=144
144 % 10 = 4
So 61679-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O/c1-7(12)11(2)9-5-3-4-8(10)6-9/h3-6H,10H2,1-2H3

61679-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-Aminophenyl)-N-methylacetamide

1.2 Other means of identification

Product number -
Other names aminophenylmethylacetamide

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:61679-27-4 SDS

61679-27-4Relevant academic research and scientific papers

PYRROLOPYRIMIDINE DERIVATIVES AS JAK3 INHIBITORS

-

, (2008/12/04)

Pyrrolopyrimidine derivatives of formula (I), wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as JAK3 kinase inhibitors.

PURINE DERIVATIVES

-

Page/Page column 70, (2008/12/07)

Purine derivatives of Formula (I), wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as JAK3 kinase inhibitors.

Metasubstituted thiazolidinones, their manufacture and use as a drug

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Page/Page column 41, (2010/11/25)

This invention involves thiazolidinone of general formula (I) and its creation and use as inhibitors of polo like kinase (PLK) for the treatment of various diseases.

Amide conformational switching induced by protonation of aromatic substituent

Yamasaki, Ryu,Tanatani, Aya,Azumaya, Isao,Saito, Shoichi,Yamaguchi, Kentaro,Kagechika, Hiroyuki

, p. 1265 - 1267 (2007/10/03)

(Matrix presented) Introduction of an electron-withdrawing group on the aromatic ring of N-methylacetanilide decreased the ratio of the cis conformer, and the ratio correlates well with the Hammett σ values of the substituents. These steric properties can be applied to achieve amide conformational swiching by protonation at the aromatic substituent of 4-[bis(dimethylamino)]-N-methylacetanilide or N-[p-(dimethylamino)phenyl]-N-phenylacetamide.

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