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2-(4-Chlorophenyl)-5-benzoxazoleacetic Acid is an organic compound that belongs to the class of 5-benzoxazolealkanoic acids. It is characterized by its pink solid appearance and is a derivative of Benoxaprofen (B165300), which is known for its anti-inflammatory properties.

51234-85-6

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51234-85-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-Chlorophenyl)-5-benzoxazoleacetic Acid is used as an active pharmaceutical ingredient for its anti-inflammatory activity. It is particularly effective in reducing inflammation and pain associated with various conditions, making it a valuable compound in the development of new medications.
Used in Chemical Research:
As a derivative of Benoxaprofen, 2-(4-Chlorophenyl)-5-benzoxazoleacetic Acid can also be used in chemical research to study the structure-activity relationship of related compounds and to develop new drugs with improved properties.
Used in Material Science:
The pink solid nature of 2-(4-Chlorophenyl)-5-benzoxazoleacetic Acid may have potential applications in material science, particularly in the development of pigments or dyes for various industries, such as textiles, plastics, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 51234-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,3 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51234-85:
(7*5)+(6*1)+(5*2)+(4*3)+(3*4)+(2*8)+(1*5)=96
96 % 10 = 6
So 51234-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClNO3/c16-11-4-2-10(3-5-11)15-17-12-7-9(8-14(18)19)1-6-13(12)20-15/h1-7H,8H2,(H,18,19)

51234-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Desmethyl Benoxaprofen

1.2 Other means of identification

Product number -
Other names 2-[2-(4-chlorophenyl)-1,3-benzoxazol-5-yl]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:51234-85-6 SDS

51234-85-6Relevant academic research and scientific papers

A FACILE SYNTHESIS OF(+/-) 2-(4-CHLOROPHENYL)-α-METHYL-5-BENZOXAZOLACETIC ACID (BENOXAPROFEN)

Huegel, Helmut M.

, p. 1075 - 1080 (2007/10/02)

A convenient four step procedure for the synthesis of benoxaprofen is described starting with 4-hydroxyphenylacetic acid.

2-Phenyl-5-benzoxazolylalkanoic acid purification process

-

, (2008/06/13)

Crude preparations of 2-phenyl-5-benzoxazolylalkanoic acids are purified by forming the ammonium salt thereof in an organic solvent and thermally reconverting the separated ammonium salt to the acid. Gaseous ammonia is a by-product.

2-(Optionally substituted)phenyl-5 or 6-substituted benzoxazoles

-

, (2008/06/13)

2-(Optionally substituted)phenyl-benzoxazoles having a carboxy alkyl, a tetrazolyl, or oxazolinyl group at the 5 or 6 position useful as aspirin-like non-steroidal, non-narcotic, analgesic, antipyretic and anti-inflammatory agents.

Benzoxazole derivatives in treating inflammation, pain and fever

-

, (2008/06/13)

The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclising an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.

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