7056-32-8

Basic information

• Product Name: Cyclohexanone, 2-hydroxy-2-[2-(2-oxocyclohexyl)ethyl]-
• CAS NO: 7056-32-8
• Molecular Formula: C14H22O3
• Molecular Weight: 238.327
• Mol File: 7056-32-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-hydroxy-2-[2-(2-oxocyclohexyl)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-hydroxy-2-[2-(2-oxocyclohexyl)ethyl]-(7056-32-8)
• EPA Substance Registry System: Cyclohexanone, 2-hydroxy-2-[2-(2-oxocyclohexyl)ethyl]-(7056-32-8)

Safety Data

• Hazardous Substances Data: 7056-32-8(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 37408-97-2 morpholinomethyl cyclohexanone hydrochloride 
• 25751-97-7 1-[2-(2-hydroxy-cyclohexyl)-ethyl]-cyclohexane-1,2-diol 
• 50-00-0 formaldehyd 
• 5396-14-5 ethyl 2-oxo-2-(2-oxocyclohexyl)acetate 
• 593-51-1 methylamine hydrochloride 
• 54599-40-5 2-(chloromethyl)cyclohexanone 
• 506-59-2 N,N-dimethylammonium chloride 
• 5331-08-8 2-(hydroxymethyl)cyclohexanone 
• 950-28-7 3,4,5,6,7,8-hexahydrospiro(chromen-2,1'-cyclohexane)-2'-one 

Downstream Products

• 25751-97-7 1-[2-(2-hydroxy-cyclohexyl)-ethyl]-cyclohexane-1,2-diol 

Relevant articles and documents

Potential antibacterial agents. Part III. Synthesis of 7-oxa-spiro [5, 9] pentadecane-1, 8, 13 trione: A novel macrocyclic lactone

In an attempt towards synthesis of intermediates (2a) 2-(1-cyanoethyl) cyclohexanone, (2b), 2-(1-nitroethyl) cyclohexanone reaction of morpholinomethyl cyclohexanone hydrochloride with CH3CN (or CH3NO2) was undetaken. Instead of the two intermediates namely 2a, 2b the known compound 3 1-(1-oxo-2-hydroxycyclohexyl)-2-(2-oxocyclohexyl)-ethane was obtained. Oxidation of this compound and its LAH reduction product 4 1-(1,2-dihydroxycyclohexyl) -2- (2- hydroxycyclohexyl) ethane with CrO3/Ac OH furnished a hitherto un-described compound 5, oxa-spiro [5,9] -pentadecane-1,8,13 trione. Its structure was established using spectroscopie techniques such as IR, HRIMS 1H-NMR, 13C-NMR etc. Antibacterial activities of the three synthesized compounds have been evaluated.