21573-70-6

Basic information

• Product Name: Methanone, 1-cyclopenten-1-ylphenyl-
• Synonyms: cyclopent-1-en-1yl phenyl ketone;cyclopent-1-enyl-phenyl ketone;1-cyclopentenyl phenyl ketone;1-benzoylcyclopent-1-ene;Cyclopent-1-enyl-phenyl-keton;Methanone,1-cyclopenten-1-ylphenyl
• CAS NO: 21573-70-6
• Molecular Formula: C12H12O
• Molecular Weight: 172.227
• Mol File: 21573-70-6.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Methanone, 1-cyclopenten-1-ylphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, 1-cyclopenten-1-ylphenyl-(21573-70-6)
• EPA Substance Registry System: Methanone, 1-cyclopenten-1-ylphenyl-(21573-70-6)

Safety Data

• Hazardous Substances Data: 21573-70-6(Hazardous Substances Data)

Upstream product

• 98-07-7 Benzotrichlorid 
• 120-92-3 cyclopentanone 
• 108201-50-9 phenyl-1-(2-methoxydiazene-1-oxide-1-yl)cyclopentyl ketone 
• 93-97-0 benzoic acid anhydride 
• 146759-05-9 cyclopent-1-en-1-yldimethyl(phenyl)silane 
• 455-32-3 benzoyl fluoride 
• 28075-49-2 1-cyclopentenyl triflate 
• 65-85-0 benzoic acid 
• 66741-06-8 N'-cyclopentylidenebenzenesulfonohydrazide 
• 33524-58-2 cyclopent-3-en-1-yl(phenyl)methanone 
• 495-41-0 1-phenylbut-2-en-1-one 
• 874338-00-8 C₁₂H₁₃BrO 
• 1254985-04-0 (6,6-diethoxy-hex-1-ynyl)benzene 
• 130602-09-4 6-phenylhex-5-yn-1-al 

Downstream Products

• 28151-83-9 (1R*,2S*)-2-benzoylcyclopentanecarboxylic acid 
• 101723-12-0 3-benzoyl-2-phenyl-cyclopentanone 
• 106596-85-4 optically inactive [trans-2-(α-hydroxy-benzyl)-cyclopentyl]-acetic acid 
• 100971-86-6 (+/-)-(trans-2-benzyl-cyclopentyl)-acetic acid 
• 105338-17-8 (6-nitro-bicyclo[3.1.0]hex-1-yl)-phenyl ketone 
• 651360-30-4 (3-bromo-2-nitro-cyclohexyl)-phenyl ketone 
• 79239-07-9 1-phenyl-1-<2-dimethyl(phenyl)silylcyclopentyl>ethanol 
• 79239-08-0 (1-(cyclopent-1-en-1-yl)ethyl)benzene 
• 123315-37-7 1-phenyl-1-(2-trimethylsilylcyclopentyl)ethanol 
• 5422-88-8 phenyl cyclopentyl ketone 
• 123315-44-6 cis-2-dimethyl(phenyl)silylcyclopentyl phenyl ketone 

Relevant articles and documents

Direct Access to α,β-Unsaturated Ketones via Rh/MgCl2-Mediated Acylation of Vinylsilanes

We report herein the facile and practical construction of α,β-unsaturated ketones via rhodium-catalyzed direct acylation of vinylsilanes with readily available and abundant carboxylic acids. This protocol features access to a diverse array of synthetically useful functionalities with moderate to excellent yields. More importantly, the late-stage functionalization of pharmaceuticals was also realized with synthetically useful yield.

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