206362-79-0

Basic information

• Product Name: 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL
• Synonyms: 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL;2-(4-CHLORO-3-FLUOROPHENYL)ETHANOL;2-(4-Chloro-3-fluorophenyl)ethan-1-ol
• CAS NO: 206362-79-0
• Molecular Formula: C8H8ClFO
• Molecular Weight: 174.6
• Mol File: 206362-79-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL(206362-79-0)
• EPA Substance Registry System: 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL(206362-79-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 206362-79-0(Hazardous Substances Data)

Usage

General Description

4-Chloro-3-fluorophenethyl alcohol is a chemical compound with the molecular formula C8H8ClFO and a molecular weight of 168.6 g/mol. It is a colorless liquid with a slightly floral odor and is primarily used as an intermediate in the production of pharmaceuticals and agrochemicals. 4-CHLORO-3-FLUOROPHENETHYL ALCOHOL is also commonly used in organic synthesis to produce various derivatives for research and development. It is important to handle this chemical with care due to its potential health hazards, as it may cause skin and eye irritation upon contact and can be harmful if ingested or inhaled.

Upstream product

• 883500-51-4 2-(4-chloro-3-fluorophenyl)acetic acid 
• 927-74-2 3-Butyn-1-ol 
• 206362-77-8 3-Chloro-4-fluorothiophene-1,1-dioxide 

Downstream Products

• 1453853-63-8 4-chloro-3-fluorophenethyl methanesulfonate 
• 1453848-23-1 1-(4-chloro-3-fluorophenethyl)-4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one 

Relevant articles and documents

3-Chloro-4-fluorothiophene-1,1-dioxide. A new synthetically useful fluorodiene

Simple, three step synthesis of a new fluorine containing diene, 3-chloro-4-fluorothiophene-1,1 -dioxide (4), from commercially available 3-sulpholene (1) has been developed. The synthetic value of compound 4 as a Diels - Alder diene has been demonstrated by its reactions with various type of dienophiles: acetylenes, alkenes, furans, quinone and anthracene. The reactions proceed with high regioselectivity to give good yields of 3-fluoro-4-chloro substituted aromatics or cyclic chlorofluorodienes. In reactions with alkenes, immediate aromatisation often occurs. In some instances, when reacted with a diene, compound 4 behaves as a dienophile.

Structural hybridization of pyrrolidine-based T-type calcium channel inhibitors and exploration of their analgesic effects in a neuropathic pain model

Highly effective and safe drugs for the treatment of neuropathic pain are urgently required and it was shown that blocking T-type calcium channels can be a promising strategy for drug development for neuropathic pain. We have developed pyrrolidine-based T