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[(4-methylphenyl)amino](phenyl)acetic acid, also known as Mefenamic acid, is a nonsteroidal anti-inflammatory drug (NSAID) that is commonly used as a pain reliever and to reduce inflammation. It belongs to the class of drugs known as fenamate and works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body.

60561-72-0

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60561-72-0 Usage

Uses

Used in Pharmaceutical Industry:
[(4-methylphenyl)amino](phenyl)acetic acid is used as an anti-inflammatory agent for the treatment of conditions involving pain and inflammation, such as menstrual pain, rheumatoid arthritis, and other similar conditions. It is effective in reducing the production of prostaglandins, which are the primary cause of pain and inflammation.
Used in Pain Management:
[(4-methylphenyl)amino](phenyl)acetic acid is used as a pain reliever to alleviate discomfort associated with various conditions, including menstrual pain and arthritis. Its ability to inhibit prostaglandin production makes it a useful option for managing pain.
Used in Oral Medication:
[(4-methylphenyl)amino](phenyl)acetic acid is used as an active ingredient in various forms of oral medication, such as tablets and capsules, for easy administration and absorption by the body.

Check Digit Verification of cas no

The CAS Registry Mumber 60561-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60561-72:
(7*6)+(6*0)+(5*5)+(4*6)+(3*1)+(2*7)+(1*2)=110
110 % 10 = 0
So 60561-72-0 is a valid CAS Registry Number.

60561-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylanilino)-2-phenylacetic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-phenyl-amino-phenyl-acetic 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:60561-72-0 SDS

60561-72-0Relevant academic research and scientific papers

A synthesis of α-amino acids via direct reductive carboxylation of imines with carbon dioxide

Sathe, Ajay A.,Hartline, Douglas R.,Radosevich, Alexander T.

, p. 5040 - 5042 (2013/06/05)

A method for the synthesis of α-amino acids by direct reductive carboxylation of aromatic imines with CO2 is described. The protocol employs readily available commercial reagents and serves as a one-step alternative to the Strecker synthesis. The Royal Society of Chemistry 2013.

ALKALOID AMINOESTER DERIVATIVES AND MEDICINAL COMPOSITION THEREOF

-

Page/Page column 214, (2010/07/09)

The present invention relates to alkaloid aminoester derivatives acting as muscarinic receptor antagonists, to methods of preparing such derivatives, to compositions comprising them and therapeutic use thereof.

Synthesis of Some New 3,4-Diarylsydnones

Csongar, Ch.,Mueller, I.,Slezak, H.,Klebsch, H.-J.,Tomaschewski, G.

, p. 1006 - 1014 (2007/10/02)

The synthesis of some new sydnones 4 is described.Their characteristic absorption maxima, mass spectroscopic fragmentation and C=O-valence vibrations are given.The sydnones 4 are synthezid by nitrosation of C,N-diarylglycines 3 (from strecker synthesis) a

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