23584-85-2

Usage

Uses

Used in Organic Synthesis:
5-PHENYL-2-(TRIFLUOROMETHYL)-3-FUROIC ACID is used as a building block in organic synthesis for its potential to contribute to the development of new compounds with various applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-PHENYL-2-(TRIFLUOROMETHYL)-3-FUROIC ACID is used as a key component in the research and development of new drugs, leveraging its pharmacological properties.
Used as a Reagent in Chemical Reactions:
5-PHENYL-2-(TRIFLUOROMETHYL)-3-FUROIC ACID serves as a reagent in chemical reactions, particularly aiding in the synthesis of a wide range of compounds.
Used in Biological Research for Anti-Inflammatory Effects:
5-PHENYL-2-(TRIFLUOROMETHYL)-3-FUROIC ACID is utilized in biological research to study its potential anti-inflammatory effects, which could lead to the development of treatments for inflammation-related conditions.
Used in Biological Research for Antifungal Effects:
Additionally, 5-PHENYL-2-(TRIFLUOROMETHYL)-3-FUROIC ACID is studied for its potential antifungal properties, which may contribute to the creation of new antifungal agents to combat fungal infections.

InChI:InChI=1/C12H7F3O3/c13-12(14,15)10-8(11(16)17)6-9(18-10)7-4-2-1-3-5-7/h1-6H,(H,16,17)

Upstream product

• 14274-07-8 methyl 3-benzoylacrylate 
• 1333158-81-8 methyl 5-phenyl-2-(trifluoromethyl)furan-3-carboxylate 

Downstream Products

• 1351960-42-3 5-phenyl-2-trifluoromethyl-furan-3-carboxylic acid (3-fluoro-5-trifluoromethyl-phenyl)-amide 

Relevant academic research and scientific papers

A powerful cascade approach for expeditious synthesis of trifluoromethylated furans

A powerful approach to synthesize trifluoromethylated furans has been developed. The method is operationally simple, broad in substrate scope, and amenable to scale-up using trifluoroacetic anhydride. Meanwhile, the strategy not only provided a versatile

FURAN OR THIOPHENE DERIVATIVE AND MEDICINAL USE THEREOF

The present invention provides a compound represented by the formula (I): [wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, p is 0, 1 or 2, and when p is 2, each R may be the same or different, R1 is a hydrogen atom or an optionally substituted hydrocarbon group, R2 is an optionally substituted aromatic group, Ring A is an optionally substituted monocyclic aromatic ring or optionally substituted bicyclic aromatic fused ring, X1 is an oxygen atom or a sulfur atom, X2 is a bond, an oxygen atom or -S(O)n- (wherein n is 0, 1 or 2), Y is a bond, an oxygen atom, -S(O)m-, -C(=O)-N(R3)- or -N(R3)-C(=O)- (R3 is a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, and m is 0, 1 or 2), M1, M2 and M3 may be the same or different and are each independently a bond or an optionally substituted divalent aliphatic hydrocarbon group, and M4 is an optionally substituted divalent aliphatic hydrocarbon group] or a salt thereof, which is useful as a prophylactic and/or therapeutic agent for lipid metabolism abnormality, arteriosclerotic disease and sequelae thereof, diabetes mellitus and the like.