1642298-59-6

Basic information

• Product Name: 3-(fluoromethyl)azetidine hydrochloride
• Synonyms: 3-(fluoromethyl)azetidine hydrochloride
• CAS NO: 1642298-59-6
• Molecular Formula: C4H9ClFN
• Molecular Weight: 125.57
• Mol File: 1642298-59-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-(fluoromethyl)azetidine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(fluoromethyl)azetidine hydrochloride(1642298-59-6)
• EPA Substance Registry System: 3-(fluoromethyl)azetidine hydrochloride(1642298-59-6)

Safety Data

• Hazardous Substances Data: 1642298-59-6(Hazardous Substances Data)

Usage

Description

3-(fluoromethyl)azetidine hydrochloride is a synthetic organic compound characterized by the presence of a fluoromethyl group attached to an azetidine ring, with a hydrochloride salt. 3-(fluoromethyl)azetidine hydrochloride is known for its potential applications in medicinal chemistry and drug development due to its unique structural features.

Uses

Used in Medicinal Chemistry:
3-(fluoromethyl)azetidine hydrochloride is used as a building block for the synthesis of more complex molecules or pharmaceutical compounds. The fluoromethyl group attached to the azetidine ring provides a versatile platform for the development of new drugs with improved pharmacological properties.
Used in Drug Development:
3-(fluoromethyl)azetidine hydrochloride is used as a precursor in the development of new pharmaceuticals. Its water-solubility and stability under various conditions make it a promising candidate for practical applications in the pharmaceutical industry, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
3-(fluoromethyl)azetidine hydrochloride is used as a subject of research to further investigate its properties and potential uses. Ongoing studies may explore its reactivity, stability, and interactions with other molecules, contributing to a deeper understanding of its role in chemistry and biology.