3183-41-3

Basic information

• Product Name: 2-ethylcycloheptan-1-one
• Synonyms: 2-ethylcycloheptan-1-one
• CAS NO: 3183-41-3
• Molecular Formula: C₉H₁₆O
• Molecular Weight: 140.22
• Mol File: 3183-41-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 205.1°Cat760mmHg
• Flash Point: 70.8°C
• Appearance: /
• Density: 0.886g/cm³
• Vapor Pressure: 0.254mmHg at 25°C
• Refractive Index: 1.44
• CAS DataBase Reference: 2-ethylcycloheptan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethylcycloheptan-1-one(3183-41-3)
• EPA Substance Registry System: 2-ethylcycloheptan-1-one(3183-41-3)

Safety Data

• Hazardous Substances Data: 3183-41-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H16O/c1-2-8-6-4-3-5-7-9(8)10/h8H,2-7H2,1H3

Upstream product

• 75-03-6 ethyl iodide 
• 502-42-1 cycloheptanone 
• 56470-75-8 2-Aethylcycloheptanol 
• 135940-64-6 (2-Ethylcycloheptan-1-on-2-yl)-carbonsaeureethylester 
• 7182-08-3 4-(1-cyclohepten-1-yl)morpholine 
• 5743-85-1 Spiro<2.6>nonan-4-one 
• 14092-11-6 1-pyrrolidino-1-cycloheptene 
• 17257-35-1 1-ethyl-cycloheptene 
• 168482-49-3 2-(1-trimethylstannylethyl)-1-cycloheptanone 
• 3183-40-2 1-(1-aminopropyl)cyclohexanol 
• 97-94-9 triethyl borane 
• 18202-04-5 2-Diazacycloheptan-1-one 
• 1121-66-0 2-Cyclohepten-1-one 
• 774-05-0 ethyl cycloheptanone-2-carboxylate 

Downstream Products

• 135940-25-9 [2-Ethyl-cyclohept-(Z)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 135940-25-9 [2-Ethyl-cyclohept-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 135971-95-8 (αS,1S,2R)-(-)-cis-2-Ethyl-N-(1-phenylethyl)cycloheptanamin-Hydrochlorid 
• 135940-25-9 [2-Ethyl-cyclohept-(Z)-ylidene]-((R)-1-phenyl-ethyl)-amine 
• 135940-25-9 [2-Ethyl-cyclohept-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine 
• 136030-06-3 (αR,1R,2S)-(+)-cis-2-Ethyl-N-(1-phenylethyl)cycloheptanamin-Hydrochlorid 

Relevant articles and documents

Further studies on 1,5-Bu3Sn group transfer reactions. 1,5-Bu3Sn group and 1,5-hydrogen atom transfer competition

1,5-Bu3Sn group transfer is favored over 1,5-hydrogen atom transfer roughly in a ratio of 20:1, 1,5-Bu3Sn transfers from carbon to carbon and from enoxy oxygen to carbon are observed for the first time.

MACROCYCLIC PYRIMIDINE DERIVATIVES

Macrocyclic pyrimidine compounds, compositions comprising such compounds, methods for making the compounds, and methods of treating and preventing the progression of diseases, conditions, and disorders using such compounds and compositions are described h

Cu-catalyzed enantioselective conjugate addition of alkylzincs to cyclic nitroalkenes: Catalytic asymmetric synthesis of cyclic α-substituted ketones

An efficient and highly enantioselective (≥92% ee) catalytic method for conjugate addition of alkylzinc reagents to cyclic nitroalkenes is reported. Reactions are promoted in the presence of 0.5-5 mol % (CuOTf)2·C6H6 and 1