5502-11-4

Basic information

• Product Name: Cyclohexanone, 3-(2-hydroxyethyl)-
• CAS NO: 5502-11-4
• Molecular Formula: C8H14O2
• Molecular Weight: 142.198
• Mol File: 5502-11-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 3-(2-hydroxyethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 3-(2-hydroxyethyl)-(5502-11-4)
• EPA Substance Registry System: Cyclohexanone, 3-(2-hydroxyethyl)-(5502-11-4)

Safety Data

• Hazardous Substances Data: 5502-11-4(Hazardous Substances Data)

Upstream product

• 930-68-7 cyclohexenone 
• 190381-03-4 3-[2'-(allyldimethylsilyl)ethyl]cyclohexan-1-one 
• 38231-56-0 methyl 2-(1,4-dioxaspiro[4.5]dec-7-yl)acetate 
• 33646-18-3 dimethyl 2-(3-oxocyclohexyl)malonate 
• 861924-46-1 2-(1,4-dioxaspiro[4.5]dec-7-yl)malonic acid dimethyl ester 
• 7076-70-2 2-(1,4-dioxaspiro[4.5]decan-7-yl)ethan-1-ol 
• 81415-36-3 2-(3-Oxo-cyclohexyl)-dithiomalonic acid di-S-ethyl ester 
• 66427-26-7 ethyl 2-(3-oxocyclohexyl)acetate 

Downstream Products

• 943448-05-3 C₁₄H₂₈O₂Si 
• 943448-07-5 5-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohex-2-en-1-one 
• 943448-06-4 C₁₇H₃₆O₂Si₂ 

Relevant articles and documents

An Approach to the Synthesis of Stenine

A type 2 N-acylnitroso intramolecular Diels-Alder reaction followed by reductive N - O bond cleavage formed the B and C rings of the Stemona alkaloid stenine. Further elaboration provided the functionalized tricyclic core.

Thiol esters in organic synthesis. X. A new approach to 1,5-ketols and 5-hydroxy esters using S,S'-diethyl dithiomalonate as an ethanol carbanion equivalent

Michael addition of S,S'-diethyl dithiomalonate to conjugated enones and α,β-unsaturated esters followed by reduction with Raney-nickel gave rise to 1,5-ketols and 5-hydroxy esters respectively in good yields.