1187930-88-6

Basic information

• Product Name: (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol
• Synonyms: (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol
• CAS NO: 1187930-88-6
• Molecular Weight: 191.1504296
• Mol File: 1187930-88-6.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol(1187930-88-6)
• EPA Substance Registry System: (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol(1187930-88-6)

Safety Data

• Hazardous Substances Data: 1187930-88-6(Hazardous Substances Data)

Usage

Description

(S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is a chemical compound with the molecular formula C8H8F3NO. It is a phenolic compound that contains a fluorinated ethylamine moiety. (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol is likely to be a synthetic intermediate or reagent used in organic synthesis or pharmaceutical research. The trifluoroethyl group can modify the reactivity and properties of the phenolic group, making this compound potentially useful in various chemical reactions and applications. Additionally, the presence of the amino group adds further versatility to its potential uses in medicinal chemistry or other fields that require the presence of a reactive amine functional group. Overall, (S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is an interesting compound with potential applications in organic synthesis and medicinal chemistry.

Uses

Used in Organic Synthesis:
(S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is used as a synthetic intermediate for the development of various organic compounds. The presence of the trifluoroethyl group and the amino group in the molecule allows for a wide range of chemical reactions, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
(S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is used as a reagent in pharmaceutical research for the development of new drugs. (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol's unique structure, which includes a phenolic group and a fluorinated ethylamine moiety, may provide novel biological activities or improve the properties of existing drug candidates. The amino group can also be used for further functionalization or modification to optimize the drug's efficacy and safety.
Used in Medicinal Chemistry:
(S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is used as a key component in the design and synthesis of new pharmaceutical agents. (S)-4-(1-aMino-2,2,2-trifluoroethyl)phenol's structural features, such as the phenolic group and the fluorinated ethylamine moiety, can be exploited to create molecules with specific biological targets or to enhance the pharmacokinetic properties of drug candidates.
Used in Chemical Reactions:
(S)-4-(1-amino-2,2,2-trifluoroethyl)phenol is used as a reactant in various chemical reactions due to its unique structural features. The trifluoroethyl group can participate in a range of reactions, such as nucleophilic substitutions, eliminations, and additions, while the amino group can be involved in reactions like acylation, alkylation, and reductive amination. This makes the compound a valuable tool for chemists working on the synthesis of novel organic compounds.