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2-(2-Methyl-6-nitrophenyl)acetic acid is a distinctive chemical compound with the molecular formula C9H9NO4. It is a member of the benzoic acids and derivatives family, characterized by a benzene ring core with a carboxylic acid substituent. 2-(2-Methyl-6-nitrophenyl)acetic acid features a 2-methyl-6-nitrophenyl group attached to an acetic acid moiety, with both the nitro and methyl groups acting as electron-attracting groups that reduce the electron density in the benzene ring. The properties and characteristics of 2-(2-Methyl-6-nitrophenyl)acetic acid are influenced by these specific chemical groups, making it valuable for a range of scientific and laboratory applications.

23876-18-8

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23876-18-8 Usage

Uses

Used in Scientific Research:
2-(2-Methyl-6-nitrophenyl)acetic acid is used as a research chemical for [application reason], contributing to the advancement of chemical and pharmaceutical studies. Its unique structure and properties make it a valuable compound for investigating various chemical reactions and processes.
Used in Laboratory Applications:
2-(2-Methyl-6-nitrophenyl)acetic acid is used as a laboratory reagent for [application reason], facilitating the execution of various experimental procedures and analyses. Its distinctive chemical properties allow for its use in a wide array of laboratory settings, enhancing the accuracy and efficiency of scientific investigations.
Used in Pharmaceutical Development:
2-(2-Methyl-6-nitrophenyl)acetic acid is used as a pharmaceutical intermediate for [application reason], playing a crucial role in the synthesis of various drugs and medications. Its presence in the development process can lead to the creation of novel therapeutic agents with potential applications in the treatment of various medical conditions.
Used in Chemical Synthesis:
2-(2-Methyl-6-nitrophenyl)acetic acid is used as a synthetic building block for [application reason], enabling the construction of more complex molecules with diverse applications. Its unique structure and reactivity make it an essential component in the synthesis of a wide range of chemical compounds, from dyes to polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 23876-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23876-18:
(7*2)+(6*3)+(5*8)+(4*7)+(3*6)+(2*1)+(1*8)=128
128 % 10 = 8
So 23876-18-8 is a valid CAS Registry Number.

23876-18-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H66654)  2-(2-Methyl-6-nitrophenyl)acetic acid, 95%   

  • 23876-18-8

  • 250mg

  • 700.0CNY

  • Detail
  • Alfa Aesar

  • (H66654)  2-(2-Methyl-6-nitrophenyl)acetic acid, 95%   

  • 23876-18-8

  • 1g

  • 2100.0CNY

  • Detail

23876-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-6-nitrophenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-METHYL-6-NITROPHENYLACETIC ACID

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:23876-18-8 SDS

23876-18-8Relevant academic research and scientific papers

Hexahydro-cyclohepta-pyrrole oxindole as potent kinase inhibitors

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Page/Page column 22, (2010/02/08)

The present invention is directed to a class indolinone compounds, hexahydro-cyclohepta-pyrrole oxindoles, which are useful as protein kinase inhibitors.

Prodrugs of a 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives

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, (2008/06/13)

The present invention relates to pyrrole substituted 2-indolinone compounds and their pharmaceutically acceptable salts which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

Combination therapy for the treatment of cancer

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, (2008/06/13)

The present invention relates to methods for treatment or prevention of neoplasia disorders using protein tyrosine kinase inhibitors in combination with cyclooxygenase inhibitors, in particular cyclooxygenase-2 selective inhibitors.

Pyrrole substituted 2-indolinone protein kinase inhibitors

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, (2008/06/13)

The present invention relates to pyrrole substituted 2-indolinone compounds and their pharmaceutically acceptable salts which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

3-heteroarylidene-2-indolinone protein kinase inhibitors

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, (2008/06/13)

The present invention relates to novel 3-heteroarylidene-2-indolinone compounds and physiologically acceptable salts thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

3-(cycloalkanoheteroarylidenyl)-2-indolinone protein tyrosine kinase inhibitors

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Page column 19-20, (2010/02/05)

The present invention relates to novel 3-(cycloalkano-heteroarylidenyl)-2-indolinone compounds and physiologically acceptable salts and prodrugs thereof which are expected to modulate the activity of protein tyrosine kinases and therefore to be useful in the prevention and treatment of protein tyrosine kinase related cellular disorders such as cancer.

3-(cycloalkanoheteroarylidenyl)-2- indolinone protein tyrosine kinase inhibitors

-

, (2008/06/13)

The present invention relates to novel 3-(cycloalkanoheteroarylidenyl)-2-indolinone compounds and physiologically acceptable salts and prodrugs thereof which are expected to modulate the activity of protein tyrosine kinases and therefore to be useful in the prevention and treatment of protein tyrosine kinase related cellular disorders such as cancer.

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