69484-34-0

Basic information

• Product Name: 2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPANOIC ACID
• Synonyms: 2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPANOIC ACID;2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPIONIC ACID;2-(4-TRIFLUOROMETHYL-PHENOXY)-PRPIONIC ACID
• CAS NO: 69484-34-0
• Molecular Formula: C₁₀H₉F₃O₃
• Molecular Weight: 234.17
• Mol File: 69484-34-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPANOIC ACID(69484-34-0)
• EPA Substance Registry System: 2-[4-(TRIFLUOROMETHYL)PHENOXY]PROPANOIC ACID(69484-34-0)

Safety Data

• Hazardous Substances Data: 69484-34-0(Hazardous Substances Data)

Usage

Physical properties

white to off-white crystalline solid, soluble in organic solvents, insoluble in water
Known for potential use as an anti-inflammatory agent
Studied for pharmacological properties
Handle with caution due to potential health hazards

Upstream product

• 402-45-9 4-hydroxybenzotrifluoride 
• 535-11-5 Ethyl 2-bromopropionate 
• 394646-83-4 ethyl (+/-)-2-(4-trifluoromethylphenoxy)propanoate 
• 598-72-1 2-Bromopropionic acid 

Downstream Products

• 253333-79-8 (R)-2-(4-trifluoromethylphenoxy)propanoic acid 
• 69183-54-6 2-(α,α,α-trifluoro-p-tolyloxy)-1-propanol 

Relevant articles and documents

HETEROCYCLIC COMPOUND

The present invention provides a compound having a PDE2A selective inhibitory action, which is useful as an agent for the prophylaxis or treatment of schizophrenia, Alzheimer's disease and the like. The present invention is a compound represented by the f

How Does Lipase Flexibility Affect Its Enantioselectivity in Organic Solvents? A Possible Role of CH...π Association in Stabilization of Enzyme-Substrate Complex

For lipase-catalyzed reactions of 2-(4-substitued phenoxy)propionic acids with alcohols in organic solvents containing a small amount of water, the increase of the lipase flexibility brought about by addition of water is found to be favorable for the indu

Microbial deracemization of alpha-substituted carboxylic acids.

An enzyme system of Nocardia diaphanozonaria JCM 3208 catalyzes the inversion of the chirality of various alpha-substituted carboxylic acids, such as 2-phenylpropanoic acid and 2-phenoxypropanoic acid derivatives, via a novel deracemization reaction.