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4-(Methylamino)-3-nitrophenyl phenyl ketone, also known as 4-Methylamino-3-nitro-benzophenone, is an organic compound that serves as an analog of the anti-parasitic drug Mebendazole (M200500). It is characterized by its unique molecular structure, which includes a nitro group and a methylamino group attached to a benzophenone backbone.

66353-71-7

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66353-71-7 Usage

Uses

Used in Pharmaceutical Industry:
4-(Methylamino)-3-nitrophenyl phenyl ketone is used as a research compound for the development of new anti-parasitic drugs. Its structural similarity to Mebendazole allows scientists to study its potential as a treatment for parasitic infections, with the aim of improving upon the efficacy and safety of existing medications.
Additionally, due to its unique chemical properties, 4-(Methylamino)-3-nitrophenyl phenyl ketone may also be utilized in the synthesis of other related compounds with potential applications in various fields, such as materials science or chemical research. However, further investigation and development are required to fully explore and understand its capabilities and limitations in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 66353-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,5 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66353-71:
(7*6)+(6*6)+(5*3)+(4*5)+(3*3)+(2*7)+(1*1)=137
137 % 10 = 7
So 66353-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O3/c1-15-12-8-7-11(9-13(12)16(18)19)14(17)10-5-3-2-4-6-10/h2-9,15H,1H3

66353-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(methylamino)-3-nitrophenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names EINECS 266-327-8

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:66353-71-7 SDS

66353-71-7Relevant academic research and scientific papers

Benz-acylbenzimidazole-2-carboxylic acid derivatives

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, (2008/06/13)

New heterocyclylcarboxylic acid derivatives which are acylated in the nucleus, especially benz-acyl-benzimidazole-2-carboxylic acid derivatives of the formula STR1 in which R is a free, esterified or amidated carboxyl group or a free, etherified or esterified hydroxymethyl group, R1 is an aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic or heterocyclic-aliphatic radical, R2 is hydrogen or an aliphatic radical and Ph is a 1,2-phenylene group containing the radical R1 --C(=O)--, with the proviso that R1 contains at least 2 carbon atoms if Ph is otherwise unsubstituted, R2 is ethyl and R is acetoxymethyl, and salts of such compounds having salt-forming properties, are useful as anti-allergic agents.

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