886371-56-8

Basic information

• Product Name: 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE
• Synonyms: 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE
• CAS NO: 886371-56-8
• Molecular Formula: C9H9F4NO
• Molecular Weight: 223.1674728
• Mol File: 886371-56-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE(886371-56-8)
• EPA Substance Registry System: 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE(886371-56-8)

Safety Data

• Hazardous Substances Data: 886371-56-8(Hazardous Substances Data)

Usage

Description

2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE is a chemical compound with the molecular formula C10H11F4NO. It is an amine derivative featuring a trifluoromethyl group and a fluoro-methoxy-phenyl group. 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE is known for its unique properties due to the presence of fluorine atoms, making it valuable for medicinal chemistry applications.

Uses

Used in Pharmaceutical Industry:
2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE is used as a building block for the synthesis of various drugs and active pharmaceutical ingredients. Its unique structure and fluorine substitution contribute to the development of new medicinal compounds with improved properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE serves as a reagent, facilitating the creation of a wide range of chemical products. Its versatility in reactions makes it an important component in the synthesis of various organic compounds.
Used in Chemical Research:
2,2,2-TRIFLUORO-1-(3-FLUORO-4-METHOXY-PHENYL)-ETHYLAMINE is also utilized in chemical research, where its properties and reactions are studied to gain insights into the behavior of fluorinated compounds and to develop new methodologies in organic chemistry.