22692-94-0

Basic information

• Product Name: Benzeneacetyl chloride, a-fluoro-
• CAS NO: 22692-94-0
• Molecular Formula: C8H6ClFO
• Molecular Weight: 172.586
• Mol File: 22692-94-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzeneacetyl chloride, a-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetyl chloride, a-fluoro-(22692-94-0)
• EPA Substance Registry System: Benzeneacetyl chloride, a-fluoro-(22692-94-0)

Safety Data

• Hazardous Substances Data: 22692-94-0(Hazardous Substances Data)

Upstream product

• 643-77-6 fluoro-phenyl-acetic acid ethyl ester 
• 774-40-3 hydroxy-phenyl-acetic acid ethyl ester 
• 17841-30-4 methyl (±)-2-fluoro-2-phenylacetate 
• 37167-62-7 bromo-phenyl-acetic acid methyl ester 
• 2835-06-5 phenylglycin 
• 1578-63-8 d'acide 2-fluoro-2-phenyl acetique 

Downstream Products

• 14865-42-0 3-(fluoro-phenyl-acetyl)-3,4-dihydro-1H-benzo[d][1,2]oxazine 
• 128864-68-6 (S)-Fluoro-phenyl-acetic acid (R)-1-methyl-2-phenyl-ethyl ester 
• 128864-68-6 (S)-Fluoro-phenyl-acetic acid (S)-1-methyl-2-phenyl-ethyl ester 
• 128864-77-7 (S)-3-((R)-2-Fluoro-2-phenyl-acetoxy)-3-phenyl-propionic acid ethyl ester 
• 128864-77-7 (S)-3-((S)-2-Fluoro-2-phenyl-acetoxy)-3-phenyl-propionic acid ethyl ester 
• 71671-72-2 t-Butyl-α-Fluorophenylperacetat 
• 13344-76-8 α-fluorobenzeneacetaldehyde 
• 22692-98-4 β-Dietilaminoetilestere dell'acido α-fluorofenilacetico 
• 22692-96-2 N-Metilanilide dell'acido α-fluorofenilacetico 
• 128864-75-5 (R)-3-((S)-2-Fluoro-2-phenyl-acetoxy)-butyric acid ethyl ester 
• 128864-75-5 (S)-3-((S)-2-Fluoro-2-phenyl-acetoxy)-butyric acid ethyl ester 
• 13659-53-5 2-fluoro-N,2-diphenylacetamide 
• 1041934-95-5 C₁₀H₁₂FNO₂ 
• 4881-22-5 phenylglyoxal bis(2,4-dinitrophenylhydrazone) 

Relevant articles and documents

AZABICYCLO AND DIAZEPINE DERIVATIVES FOR TREATING OCULAR DISORDERS

The present invention provides in one aspect azabicycio and diazepine derivatives useful as modulators of muscarinic receptors. In another aspect, the present invention provides pharmaceutical compositions for treating ocular diseases, the compositions comprising at least one muscarinic receptor modulator. Formulae (I) & (II):

The in situ generation and trapping of some fluorine-substituted ketenes

Fluoroketene, difluoroketene, methylfluoroketene, trifluoromethylfluoroketene, and phenylfluoroketene were each generated, in situ, via dehydrohalogenation of the respective acid chlorides. In the presence of cyclopentadiene [2 + 2] adducts were obtained in all but the difluoroketene case. In the absence of cyclopentadiene, low temperature 19F nmr indicated the presence of acyl ammonium salts and enolates, potential precursors of the ketenes, but no actual ketene species could unambiguously be detected. The stereochemical results were consistent with the currently accepted steric-based mechanistic rationale for stereochemical determination in ketene cycloadditions.

Fluorinated organic compounds with potential biological activity. VII. (1) N-substituted amides of alpha-fluoroarylacetic acid

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