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p-Chloro-methylphenyl acetic acid, also known as 4-Chloromethylphenylacetic acid, is a chemical compound with the molecular formula C9H9ClO2. It is a white crystalline solid with a melting point of around 65-68°C. p-Chloro-methylphenyl acetic acid is recognized for its versatile applications in pharmaceutical chemistry, particularly due to its anti-inflammatory and analgesic properties, as well as its role as a potent inhibitor of cyclooxygenase, an enzyme involved in the production of inflammatory mediators.

56066-91-2

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56066-91-2 Usage

Uses

Used in Pharmaceutical Industry:
p-Chloro-methylphenyl acetic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of medications with anti-inflammatory and analgesic effects. Its role in inhibiting cyclooxygenase makes it a valuable component in the creation of drugs aimed at treating conditions like rheumatoid arthritis and other inflammatory disorders.
Used in Agrochemical Industry:
Although the provided materials do not explicitly mention its use in agrochemicals, p-Chloro-methylphenyl acetic acid's common use as an intermediate in the synthesis of agrochemicals suggests that it may be utilized in the development of products for agricultural applications, potentially including pesticides or herbicides, due to its chemical properties.
Used in Inflammatory Condition Treatment:
p-Chloro-methylphenyl acetic acid is used as a potential treatment for inflammatory conditions such as rheumatoid arthritis, leveraging its anti-inflammatory and analgesic properties to alleviate symptoms and improve patient outcomes.
Used in Enzyme Inhibition Studies:
As a potent inhibitor of cyclooxygenase, p-Chloro-methylphenyl acetic acid is used in research and development for studying enzyme inhibition mechanisms, which can be crucial for understanding and treating a variety of inflammatory and pain-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 56066-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56066-91:
(7*5)+(6*6)+(5*0)+(4*6)+(3*6)+(2*9)+(1*1)=132
132 % 10 = 2
So 56066-91-2 is a valid CAS Registry Number.

56066-91-2SDS

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-(Chloromethyl)phenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-[4-(chloromethyl)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:56066-91-2 SDS

56066-91-2Relevant academic research and scientific papers

Ketonization of the unusually acidic elongated enol generated by flash photolytic decarboxylation of p-formylphenylacetic acid in aqueous solution

Chiang, Yvonne,Kolmakov, Kirill,Kresge, A. Jerry

, p. 101 - 104 (2008/09/18)

Rates of photolysis of p-formylphenylacetic acid were measured flash photoytically in perchloric acid and sodium, hydroxide solutions, and also in acetic acid, biphosphate ion, and tris-(hydroxym.ethyl)methaneam.monium ion buffers, using H2O and D2O as solvents. The results provide rate profiles and solvent isotope effects, which indicate that photolysis occurs through an elongated enol intermediate. This enol is unusually strongly acidic, by some two to three pQa units, when compared with simple non-elongated enols.

Triazole derivatives

-

, (2011/03/17)

The present invention relates to triazole and imidazole derivatives of formula I and to their pharmaceutically acceptable acid addition salts. These compounds are NMDA receptor subtype blockers and are useful for the treatment of diseases related to the NMDA receptor.

trans-4-Stilbenecarboxylatoalkylpentaamminecobalt(III) perchlorates: Synthesis and intramolecular energy transfer

Parkanyi, Cyril,Huang, Lois Shiow-Chyn Yeh,Chu, Sung Gun,Jeffries III, Alfred T.

, p. 342 - 354 (2007/10/03)

Three homologs of tran-4-stilbenecarboxylic acid, viz., trans-4-stilbeneacetic acid (18), β-(trans-4-stilbene)propionic acid (19), and γ-trans-4-stilbene)butyric acid (20) were synthesized and, together with the parent trans-4-stilbenecarboxylic acid, use

A Novel Receptor for Dicarboxylic Acid Derivatives

Flack, Stephen S.,Chaumette, Jean-Louis,Kilburn, Jeremy D.,Langley, G. John,Webster, Michael

, p. 399 - 401 (2007/10/02)

A novel receptor 4 has been prepared, which binds the monopotassium salts of various dicarboxylic acids in chloroform solution, using a combination of hydrogen bonding interactions and an electrostatic association between a carboxylate anion and a crown e

Cephalosporin antibiotics

-

, (2008/06/13)

Novel cephalosporin antibiotic derivatives.

Cephalosporin antibiotics

-

, (2008/06/13)

Novel cephalosporin antibiotic derivatives.

Cephalosporin antibiotics

-

, (2008/06/13)

Novel cephalosporin antibiotic derivatives.

Isothiourea substituted cephalosporin derivatives

-

, (2008/06/13)

Novel cephalosporin and penicillin antibiotic derivatives.

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