458-04-8

Usage

Uses

Used in Pharmaceutical Industry:
3-Fluorophenylacetyl chloride is used as a building block for the synthesis of various pharmaceuticals, leveraging its reactivity to form complex organic compounds that can exhibit therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Fluorophenylacetyl chloride serves as a key intermediate in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used in Dye and Pigment Manufacturing:
3-Fluorophenylacetyl chloride is utilized as an intermediate in the production of dyes and pigments, contributing to the development of colorants for a variety of applications.
Used in Fine Chemicals Production:
3-FLUOROPHENYLACETYL CHLORIDE is also employed in the manufacturing of other fine chemicals, where its reactive nature is harnessed to produce specialty chemicals for specific industrial uses.
Each application takes advantage of 3-Fluorophenylacetyl chloride's unique chemical properties to fulfill the requirements of different industries, underscoring its versatility and importance in chemical synthesis and compound development.

InChI:InChI=1/C8H6ClFO/c9-8(11)5-6-2-1-3-7(10)4-6/h1-4H,5H2

Upstream product

• 352-70-5 m-Fluorotoluene 
• 456-41-7 1-(Bromomethyl)-3-fluorobenzene 
• 501-00-8 3-fluorophenylacetonitrile 
• 1711-07-5 3-fluorobenzoyl chloride 
• 6929-49-3 m-Fluoro-ω-diazoacetophenon 
• 455-38-9 3-fluorobenzoic acid 

Downstream Products

• 2711-92-4 (3-fluoro-phenyl)-acetic acid-(2-piperidino-ethyl ester) 
• 153529-18-1 2-(3-Fluoro-phenyl)-1-(4-methoxy-phenyl)-ethanone 
• 29419-15-6 7-fluoro-1,2,3,4-tetrahydronaphthalen-2-one 
• 548771-68-2 5-fluoro-2-tetralone 
• 143659-28-3 1-Naphthylmethyl 3-fluorophenylacetate 
• 162939-91-5 4-{4-[2-(3-Fluoro-phenyl)-acetyl]-phenyl}-butyric acid methyl ester 
• 423184-26-3 1-diazo-3-(3-fluoro-phenyl)-propan-2-one 
• 1211978-41-4 C₁₆H₁₁FO₂ 
• 1403776-43-1 C₁₉H₁₅F₂N₃O₂ 
• 1353578-36-5 C₁₃H₁₇F 
• 1353578-38-7 C₁₃H₁₆FI 
• 926226-12-2 C₁₂H₁₅FN₂O 
• 1094313-25-3 1-(4-chlorophenyl)-2-(3-fluorophenyl)ethan-1-one 

Relevant academic research and scientific papers

N-SULFONYL THIAZOLYLPIPERAZINE DERIVATIVES AND RELATED N-SULFONYL HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF NEURO DEGENERATIVE DISEASES

This invention provides thiazolylpiperazine derivatives, and N-sulfonyl heterocyclic derivatives including phenyl- and benzyl-thiazolylpiperidine derivatives, and pharmaceutically acceptable salts thereof, which are useful active ingredients for administration in a method for the treatment of an α-synucleopathy such as Parkinson's disease, diffuse Lewy body disease, traumatic brain injury, amyotrophic lateral sclerosis, Niemann-Pick disease, Hallervorden-Spatz syndrome, Down syndrome, neuroaxonal dystrophy, multiple system atrophy and Alzheimer's disease. This invention also provides methods for making such derivatives, and pharmaceutical compositions including such derivatives together with pharmaceutically acceptable excipients.

SUBSTITUTED PYRIDINE DERIVATIVES AND THEIR MEDICAL USE

The present application discloses novel substituted 1,4-oxazepanyl-pyridine derivatives and their use as modulators of the voltage gated KV7 (KCNQ) potassium ion channels. In other aspects the application discloses the use of these compounds, i

PHENOXYACETIC ACID DERIVATIVES USEFUL FOR TREATING RESPIRATORY DISEASES

The invention relates to substituted phenoxyacetic acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.Formula (I)

SUBSTITUTED MORPHOLINE AND THIOMORPHOLINE DERIVATIVES

The present invention relates to morpholine and thiomorpholine derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.