332-43-4

Usage

Uses

4-Fluorophenethyl Chloride can be used as a bactericide.

InChI:InChI=1/C8H8ClF/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6H2

Upstream product

• 7589-27-7 2-(4-Fluorophenyl)ethanol 
• 352-13-6 4-flourophenylmagnesium bromide 
• 858855-90-0 4-aminophenethyl benzoate 
• 84648-18-0 C₁₆H₁₂ClFO₄ 
• 326-46-5 2-(4-fluorophenyl)ethyl benzoate 

Downstream Products

• 459-19-8 2-(4-fluorophenyl)ethylamine hydrochloride 
• 823189-01-1 1-(2-azidoethyl)-4-fluorobenzene 
• 164179-52-6 1-iodo-2-(4-fluorophenyl)ethane 
• 126570-62-5 N-(1,1-DIMETHYLETHYL)-3-[3-(4-FLUOROPHENYL)PROPYL]-5-METHYL-2-PYRIDINE CARBOXAMIDE 
• 1065498-70-5 2-(2-(4-fluorophenyl)ethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 459-47-2 1-ethyl-4-fluorobenzene 
• 126534-42-7 (S)-1-chloro-2-hydroxy-2-(p-fluorophenyl)ethane 
• 126534-43-8 [R]-1-chloro-2-(4-fluorophenyl)-2-ethanol 
• 455267-24-0 C-{1-[2-(4-Fluoro-phenyl)-ethanesulfonyl]-piperidin-4-yl}-methylamine 
• 1584657-15-7 1-chloro-4-(((4-fluorophenethyl)sulfonyl)methyl)benzene 

Relevant academic research and scientific papers

Cascade bio-hydroxylation and dehalogenation for one-pot enantioselective synthesis of optically active β-halohydrins from halohydrocarbons

A stereoselective hydroxylation and enantioselective dehalogenation cascade reaction was developed for the synthesis of optically active β-haloalcohols from halohydrocarbons. This cascade system employed P450 and halohydrin dehalogenase as two compatible biocatalysts, allowing a straightforward, greener and efficient access to β-halohydrins with excellent enantioselectivities (98-99%).

N-substituted nonaryl-heterocyclo amidyl NMDA/NR2B Antagonists

Compounds represented by Formula (I): or pharmaceutically acceptable salts thereof, are effective as NMDA NR2B antagonists useful for relieving pain.

N-substituted nonaryl-heterocyclic NMDA/NR2B antagonists

Compounds represented by Formula (I): 1or pharmaceutically acceptable salts thereof, are effective as NMDA NR2B antagonists useful for relieving pain.

Compounds having a plurality of nitrogenous substitutents

Novel compounds having the formula: STR1wherein the constituent variables are defined herein. The compounds are constructed to include a central aromatic, aliphatic, or heterocyclic ring system. Attached to the central ring system are two linear groups having nitrogenous moieties that are derivatized with chemical functional groups. The ring system can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring, that may also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the these compounds. In accordance with certain embodiments of the invention, libraries of such compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the libraries.

Structure of ω-Arylalkyl Radicals: A 13C CIDNP Investigation

Thermolysis of a series of ω-arylalkanoyl m-chlorobenzoyl (and acetyl) peroxides at ca. 100 deg C in cyclohexanone and in hexachloroacetone was studied by using 13C chemically induced dynamic nuclear polarization.Analysis of the observed 13C polarizations indicate that all the three radicals (β-arylethyl, γ-arylpropyl and δ-arylbutyl) have open-chain structures with no evidence for aryl participation resulting in spirocycloalkylcyclohexadienyl radicals.