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N-(5-CHLORO-4-METHYL-2-NITROPHENYL)ACETAMIDE is a chemical compound characterized by the molecular formula C8H8ClN2O3. It is an organic compound that exhibits a yellow to brownish crystalline appearance. N-(5-CHLORO-4-METHYL-2-NITROPHENYL)ACETAMIDE is recognized for its potential as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it may also hold promise in the fields of medicine and organic chemistry due to its structural properties and reactivity. Careful handling and storage are essential to prevent harm from ingestion, inhalation, or skin contact.

7149-78-2

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7149-78-2 Usage

Uses

Used in Pharmaceutical Synthesis:
N-(5-CHLORO-4-METHYL-2-NITROPHENYL)ACETAMIDE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex organic molecules that can have therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, N-(5-CHLORO-4-METHYL-2-NITROPHENYL)ACETAMIDE is utilized as an intermediate in the production of compounds that can help protect crops from pests and diseases, leveraging its reactivity in chemical reactions to create effective agrochemicals.
Used in Organic Chemistry Research:
Due to its unique structural properties and reactivity, N-(5-CHLORO-4-METHYL-2-NITROPHENYL)ACETAMIDE is employed in organic chemistry research to explore new reactions and syntheses, potentially leading to the discovery of novel compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7149-78-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7149-78:
(6*7)+(5*1)+(4*4)+(3*9)+(2*7)+(1*8)=112
112 % 10 = 2
So 7149-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O3/c1-5-3-9(12(14)15)8(4-7(5)10)11-6(2)13/h3-4H,1-2H3,(H,11,13)

7149-78-2SDS

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 N-(5-Chloro-4-methyl-2-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names acetic acid-(5-chloro-4-methyl-2-nitro-anilide)

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:7149-78-2 SDS

7149-78-2Relevant academic research and scientific papers

MICROSOMAL PROSTAGLANDIN E SYNTHASE-1 (MPGES1) INHIBITORS

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Page/Page column 164, (2011/04/14)

A compound of formula (I): as well as pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising the compound. The compound is useful for the treatment of disorder selected from inflammatory diseases, nociceptive pain, auto-imm

FLAVIN DERIVATIVES

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Page/Page column 167, (2010/04/03)

The present invention relates novel flavin derivatives and other flavin derivatives, their use and compositions for use as riboswitch ligands and/or anti-infectives. The invention also provides method of making novel flavin derivatives.

Cardiotonic Agents. Synthesis and Cardiovascular Properties of Novel 2-Arylbenzimidazoles and Azabenzimidazoles

Guengoer, Timur,Fouquet, Andre,Teulon, Jean-Marie,Provost, Daniel,Cazes, Michele,et al.

, p. 4455 - 4463 (2007/10/02)

Novel 2-arylbenzimidazoles and azabenzimidazoles were synthesized, and their inotropic action was evaluated.Changes in left ventricular pressure, dP/dt max, were measured as an index of cardiac contractility.The structural features that impart optimal inotropic activity are presented.The most potent compounds were evaluated orally in conscious dogs with implanted Konigsberg pressure transducers.To investigate the mechanism of action, the most potent compounds were tested for their calcium-sensitizing properties and their potential for the inhibition of phosphodiesterase.Two compounds, 1 and 41, showed interesting in vitro and oral activity without side effects.They have a more potent calcium-sensitizing effect than MCI-154 and are under further investigation.

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