1124-90-9

Basic information

• Product Name: 1-Propanone, 1-(1-hydroxycyclohexyl)-
• CAS NO: 1124-90-9
• Molecular Formula: C9H16O2
• Molecular Weight: 156.225
• Mol File: 1124-90-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(1-hydroxycyclohexyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(1-hydroxycyclohexyl)-(1124-90-9)
• EPA Substance Registry System: 1-Propanone, 1-(1-hydroxycyclohexyl)-(1124-90-9)

Safety Data

• Hazardous Substances Data: 1124-90-9(Hazardous Substances Data)

Upstream product

• 22082-46-8 1-(1'-hydroxycyclohexyl)-2-propen-1-one 
• 79-03-8 propionyl chloride 
• 108-94-1 cyclohexanone 
• 697-37-0 1-(1-propynyl)cyclohexanol 
• 1123-86-0 cyclohexyl ethyl ketone 
• 931-97-5 1-hydroxy-1-cyclohexanecarbonitrile 
• 3277-89-2 phenethylmagnesium bromide 
• 24731-36-0 1-trimethylsilanyloxycyclohexanecarbonitrile 
• 107-12-0 propiononitrile 
• 67306-93-8 N-tert-Butyl-N'-prop-(Z)-ylidene-hydrazine 
• 62737-41-1 DL-2-dimethylamino-butyronitrile 
• 1206-23-1 1-tetrahydropyran-2-yloxy-cyclohexanecarbonitrile 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 1142-69-4 1-<1-Hydroxy-1-phenyl-propyl>-cyclohexanol-(1) 
• 1197-71-3 (+/-)-1-Hydroxy-1-(1-hydroxy-1-methyl-propyl)-cyclohexan 
• 1124-89-6 1-(α-Oxy-propyl)-cyclohexanol-(1) 

Relevant articles and documents

Efficient synthesis of tertiary α-hydroxy ketones through CO 2-promoted regioselective hydration of propargylic alcohols

A carbon dioxide-promoted and silver acetate-catalyzed hydration of propargylic alcohols for the efficient synthesis of tertiary α-hydroxy ketones has been developed. The reaction is proposed to proceed via a tandem process of carbon dioxide incorporation into propargylic alcohols and subsequent hydrolysis. This journal is the Partner Organisations 2014.

Synthesis of α-Hydroxy Ketones by Samarium(II) Iodide-Mediated Coupling of Organic Halides, an Isocyanide, and Carbonyl Compounds

A new strategy for the synthesis of α-hydroxy ketones by samarium(II) iodide-mediated three-component coupling of organic halides, an isocyanide, and carbonyl compounds is disclosed.An (α-iminoalkyl)samarium(III) species is generated in situ by treatment

SYNTHESIS OF 1,2-GLYCOL MONOETHERS UTILIZING DECARBONYLATION OF α-ALKOXYACID CHLORIDES MEDIATED BY SAMARIUM DIIODIDE

A new synthesis of 1,2-glycol monoethers has been achived by utilizing decarbonylation of α-alkoxyacid chlorides mediated by samarium diiodide in the presence of ketones.This one-pot reaction works within a few minutes at room temperature.The structure of α-alkoxyacid chlorides (R2,R3)C(OR1)COCl2 tolerates various substitution patterns (R2=R3=H; R2=H; R3=Me or R2=R3=Me).