155854-96-9

Basic information

• Product Name: (2-Benzylcycloheptan-1-on-2-yl)-carbonsaeureethylester
• Synonyms: (2-Benzylcycloheptan-1-on-2-yl)-carbonsaeureethylester
• CAS NO: 155854-96-9
• Molecular Weight: 274.36
• Mol File: 155854-96-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2-Benzylcycloheptan-1-on-2-yl)-carbonsaeureethylester(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Benzylcycloheptan-1-on-2-yl)-carbonsaeureethylester(155854-96-9)
• EPA Substance Registry System: (2-Benzylcycloheptan-1-on-2-yl)-carbonsaeureethylester(155854-96-9)

Safety Data

• Hazardous Substances Data: 155854-96-9(Hazardous Substances Data)

Upstream product

• 774-05-0 ethyl cycloheptanone-2-carboxylate 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 

Downstream Products

• 87722-64-3 (+/-)-2-benzylcycloheptanone 
• 155854-97-0 2-Benzyl-1-methylenecycloheptane 
• 155855-01-9 2-Benzyl-1-(hydroxymethyl)cycloheptane 
• 155855-03-1 2-Benzyl-cycloheptanecarboxylic acid 
• 133519-97-8 (1R,2R)-(+)-cis-2-Cyclohexylmethylcycloheptanamin-Hydrochlorid 
• 135940-33-9 [2-Benzyl-cyclohept-(Z)-ylidene]-((R)-1-phenyl-ethyl)-amine 
• 135940-33-9 [2-Benzyl-cyclohept-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine 
• 135940-33-9 [2-Benzyl-cyclohept-(Z)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 135940-33-9 [2-Benzyl-cyclohept-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 136030-12-1 (1R,2R)-(+)-cis-2-Benzylcycloheptanamin-Hydrochlorid 
• 133519-96-7 (1S,2S)-(-)-cis-2-Benzylcycloheptanamin-Hydrochlorid 
• 136030-08-5 (αR,1R,2R)-(+)-cis-2-Benzyl-N-(1-phenylethyl)cycloheptanamin-Hydrochlorid 
• 135971-97-0 (αS,1S,2S)-(-)-cis-2-Benzyl-N-(1-phenylethyl)cycloheptanamin-Hydrochlorid 

Relevant articles and documents

Regioselective Aryl Radical Cyclization. 1. Stereocontrolled Synthesis of Linearly Condensed Hydroaromatic Carbocyclic Systems through 6-endo-ring Closures

The stereocontrolled synthesis of trans-octahydroanthracenes 3, 11a-c, and 14a-c and trans-octahydro-5aH-cycloheptanaphthalene (27) through implementation of an efficient and highly regioselective 6-endo-trig-aryl radical cyclization of the respective 2-(o-bromoaryl)-1-methylenecyclohexanes 2, 10a-c, and 13a-c and 2-(o-bromobenzyl)-1-methylenecycloheptane (41) with tri-n-butyltin hydride id described.The radical cyclization of 2-(o-bromobenzyl)-1-methylenecyclopentane (43), in contrast, produced a mixture of the cis- and trans-hexahydro-1H-benzindenes (38) and (37).