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2-(4-METHOXY-2-METHYLPHENYL)ACETIC ACID, also known as o-methyl-4-methoxy-alpha-tolylacetic acid, is a chemical compound with the molecular formula C10H12O3. It is derived from the aromatic compound toluene and contains both a methoxy and a methyl group. This crystalline solid, which is white to off-white in color, is slightly soluble in water. It is recognized for its potential analgesic and anti-inflammatory properties, making it a promising target for drug development and research.

942-97-2

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942-97-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-METHOXY-2-METHYLPHENYL)ACETIC ACID is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Drug Development and Research:
2-(4-METHOXY-2-METHYLPHENYL)ACETIC ACID is used as a target for drug development and research due to its potential analgesic and anti-inflammatory properties. Its ability to alleviate pain and reduce inflammation makes it a candidate for the creation of new medications to treat various conditions.
Used in Organic Compounds Synthesis:
2-(4-METHOXY-2-METHYLPHENYL)ACETIC ACID is used as a key component in the synthesis of a wide range of organic compounds. Its versatility in chemical reactions allows it to be incorporated into various molecules with different applications across multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 942-97-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 942-97:
(5*9)+(4*4)+(3*2)+(2*9)+(1*7)=92
92 % 10 = 2
So 942-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-7-5-9(13-2)4-3-8(7)6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)

942-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxy-2-methylphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-NITROPHENYL)-1H-BENZIMIDAZOLE-5-CARBOXYLIC 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:942-97-2 SDS

942-97-2Relevant academic research and scientific papers

Carboxylation of benzylic and aliphatic C-H bonds with CO2 induced by light/ketone/nickel

Ishida, Naoki,Masuda, Yusuke,Imamura, Yuuya,Yamazaki, Katsushi,Murakami, Masahiro

supporting information, p. 19611 - 19615 (2019/12/24)

A photoinduced carboxylation reaction of benzylic and aliphatic C-H bonds with CO2 is developed. Toluene derivatives capture gaseous CO2 at the benzylic position to produce phenylacetic acid derivatives when irradiated with UV light in the presence of an aromatic ketone, a nickel complex, and potassium tert-butoxide. Cyclohexane reacts with CO2 to furnish cyclohexanecar-boxylic acid under analogous reaction conditions. The present photoinduced carboxylation reaction provides a direct access from readily available hydrocarbons to the corresponding carboxylic acids with one carbon extension.

Synthesis of 4-Hydroxy-2-methylbenzoic Acid and Its Higher Homologues

Sen, P. K.,Pal, Panchanan,Goswami, Shyamaprosad,Chattopadhyay, Gautam

, p. 679 - 682 (2007/10/02)

Synthesis of 4-hydroxy-2-methylbenzoic acid (1a) and its higher homologues such as 4-hydroxy-2-methylphenylacetic acid (1b), 3-(4-hydroxy-2-methylphenyl)propanoic acid (1c) and 4-(4-hydroxy-2-methylphenyl)butanoic acid (1d) are described.

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