52329-71-2

Basic information

• Product Name: Cyclohexanecarboxaldehyde, 1-hydroxy-
• CAS NO: 52329-71-2
• Molecular Formula: C7H12O2
• Molecular Weight: 128.171
• Mol File: 52329-71-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Cyclohexanecarboxaldehyde, 1-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxaldehyde, 1-hydroxy-(52329-71-2)
• EPA Substance Registry System: Cyclohexanecarboxaldehyde, 1-hydroxy-(52329-71-2)

Safety Data

• Hazardous Substances Data: 52329-71-2(Hazardous Substances Data)

Upstream product

• 42186-00-5 4-ethoxy-1-oxa-3-aza-spiro[4.5]dec-2-ene 
• 5849-22-9 2-(1-hydroxycyclohexyl)-1,3-dithiane 
• 39922-36-6 Cyclohexylidenmethylphosphonsaeurediaethylester 
• 24731-36-0 1-trimethylsilanyloxycyclohexanecarbonitrile 
• 126227-79-0 1-[(Dimethyl-phenyl-silanyl)-methoxy-methyl]-cyclohexanol 
• 135879-95-7 1-trimethylsiloxycyclohexanecarbaldehyde 
• 103722-10-7 2-Chloromethanesulfonyl-1-oxa-spiro[2.5]octane 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 108-94-1 cyclohexanone 
• 1940-19-8 1-vinylcyclohexanol 

Downstream Products

• 98-89-5 Cyclohexanecarboxylic acid 
• 89036-95-3 1-hydroxycyclohexancarboxaldehyde dimethyl acetal 
• 15419-46-2 1-formylcyclohexene 2,4-dinitrophenylhydrazone 
• 1123-28-0 1-hydroxy-cyclohexanecarboxylic acid 
• 4436-58-2 2-hydroxycyloheptanone 
• 15753-47-6 1-(hydroxymethyl)cyclohexanol 
• 1309387-69-6 1-(1-hydroxy-cyclohexyl)-hex-2-yne-1,6-diol 
• 1309387-86-7 1-[6-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-hex-2-ynyl]-cyclohexanol 
• 79224-48-9 Acetic acid 1-(acetoxy-cyano-methyl)-cyclohexyl ester 
• 79224-37-6 1-Hydroxy-1-<1-hydroxy-cyclohexyl-(1)>-acetonitril 

Relevant articles and documents

A highly efficient access to spiroketals, mono-unsaturated spiroketals, and furans: Hg(II)-catalyzed cyclization of alkyne diols and triols

Hg(II) salts are identified as highly efficient catalysts for the versatile construction of spiroketals from alkyne diols in aqueous conditions. Monounsaturated spiroketals and furans were accessed with equal ease when propargylic triols (or propargylic d

Reduction of α-Trialkylsiloxy Nitriles with Diisobutylaluminium Hydride (DIBAH): A Facile Preparation of α-Trialkylsiloxy Aldehydes and their Derivatives

The stepwise synthesis of α-trimethylsiloxy aldehydes and α-hydroxy aldehydes could be achieved via the reduction of α-trimethylsiloxy nitriles with diisobutylaluminium hydride (DIBAH) starting from a variety of ketones.The facile synthesis of optically active α-tert-butyldimethylsiloxy aldehydes was attained by combination of asymmetric silylcyanation of aldehydes and DIBAH reduction of optically active α-siloxy nitriles.Furthermore, in the reduction of some α-tert-butyldimethylsiloxy-β,γ-unsaturated nitriles, migration of the double bond took place to form more stable α-siloxy-α,β-unsaturated aldehydes under some reaction conditions.

Benzotriazol-1-ylmethyl isocyanide, a new synthon for CH-N=C transfer. Syntheses of α-hydroxyaldehydes, 4-ethoxy-2-oxazolines and oxazoles

Readily prepared benzotriazol-1-ylmethyl isocyanide (BetMIC) reacts under mild conditions with ketones and aldehydes, to afford oxazolines (convertible into α-hydroxyaldehydes) and oxazoles, respectively.