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2-(2-thienyl)propionic acid, also known as tiaprofenic acid, is an organic compound with the chemical formula C8H8O2S. It belongs to the class of nonsteroidal anti-inflammatory drugs (NSAIDs) and is used for its analgesic and anti-inflammatory properties.
Used in Pharmaceutical Industry:
2-(2-thienyl)propionic acid is used as an analgesic and anti-inflammatory agent for the treatment of conditions such as arthritis and menstrual cramps. It works by inhibiting the production of certain natural substances in the body that cause inflammation and pain, providing relief to patients suffering from these conditions.
Used in Pain Management:
2-(2-thienyl)propionic acid is used as a pain reliever to alleviate discomfort caused by various conditions, including but not limited to arthritis and menstrual cramps. Its effectiveness in reducing pain can improve the quality of life for individuals experiencing chronic or acute pain.
Used in Inflammation Reduction:
2-(2-thienyl)propionic acid is used as an anti-inflammatory agent to reduce inflammation in the body. By inhibiting the production of substances that cause inflammation, it can help manage the symptoms of inflammatory conditions and promote healing.

54955-39-4

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54955-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54955-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54955-39:
(7*5)+(6*4)+(5*9)+(4*5)+(3*5)+(2*3)+(1*9)=154
154 % 10 = 4
So 54955-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2S/c1-5(7(8)9)6-3-2-4-10-6/h2-5H,1H3,(H,8,9)

54955-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-thiophen-2-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names 2-Thiopheneacetic acid,a-methyl

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:54955-39-4 SDS

54955-39-4Upstream product

54955-39-4Relevant articles and documents

Synthetic process of tiaprofenic acid

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, (2018/04/01)

The invention relates to a synthetic process of tiaprofenic acid. The synthetic process comprises the following steps: adopting 2-thiotolene as a starting raw material, enabling 2-thiotolene to reactwith trimethylsilyl cyanide to synthesize 2-thiopheneacetonitrile by virtue of bromation, then enabling the 2-thiopheneacetonitrile to react with dimethyl carbonate to be methylated, hydrolyzing cyanogroups, and finally performing F-K reaction with benzoyl chloride, and preparing tiaprofenic acid. The synthetic process has the advantages that the conventional safe raw materials low in price are used for substituting the rare expensive and dangerous raw materials, so that the severe pollution problem is avoided, and the production cost is greatly decreased; and in addition, the process route adopted by the invention is simple, the reaction period is short, the reaction condition is stable, the yield is high and can reach more than 90 percent, the produce obtained after the reaction is highin purity, and the purity can reach more than 99 percent, so that the synthetic process is suitable for the industrialized production.

Process for the preparation of arylalkanoic acids by oxidative rearrangement of arylalkanones

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, (2008/06/13)

Process for preparing an arylalkanoic acid by adding iodine to a mixture of an arylalkanone and an excess of an orthoester, heating of the mixture thus obtained, adding an inorganic base and finally an acid.

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