53723-51-6

Basic information

• Product Name: 1-Cyclohexene-1-methanol, acetate
• CAS NO: 53723-51-6
• Molecular Formula: C9H14O2
• Molecular Weight: 154.209
• Mol File: 53723-51-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Cyclohexene-1-methanol, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexene-1-methanol, acetate(53723-51-6)
• EPA Substance Registry System: 1-Cyclohexene-1-methanol, acetate(53723-51-6)

Safety Data

• Hazardous Substances Data: 53723-51-6(Hazardous Substances Data)

Upstream product

• 104178-78-1 1-acetoxy-1-acetoxymethyl-cyclohexane 
• 4845-04-9 1-cyclohexene-1-methanol 
• 108-24-7 acetic anhydride 
• 33867-02-6 1-chloromethylcyclohexene 
• 64-19-7 acetic acid 
• 1192-37-6 methylenecyclohexane 
• 94421-40-6 Acetic acid 1-nitro-2-phenylsulfanyl-cyclohexylmethyl ester 
• 75-36-5 acetyl chloride 
• 94421-39-3 (1-Nitro-2-phenylsulfanyl-cyclohexyl)-methanol 
• 15753-47-6 1-(hydroxymethyl)cyclohexanol 

Downstream Products

• 4845-04-9 1-cyclohexene-1-methanol 
• 341028-78-2 2-(2-Methylene-cyclohexyl)-propionic acid methyl ester 
• 63715-04-8 3-Cyclohex-1-enyl-2-methyl-propionic acid methyl ester 
• 1192-88-7 1-cyclohexene-1-carboxaldehyde 
• 354578-83-9 (6-hydroxycyclohex-1-en-1-yl)methyl acetate 
• 412010-93-6 diphenyl-acetic acid-(cyclohex-1-enylmethyl ester) 
• 71518-98-4 2-chloro-1-methylenecyclohexane 
• 38970-47-7 2-(2-methylenecyclohexyl)acetic acid 
• 133967-35-8 3-Cyclohex-1-enyl-2-phenyl-propionic acid methyl ester 
• 54445-54-4 (+/-)-methyl 2-methylene-1-cyclohexaneacetate 
• 54445-57-7 methyl 3-(1-cyclohexenyl) propanoate 

Relevant articles and documents

Synthesis and comparative antibacterial activity of verdamicin C2 and C2a. A new oxidation of primary allylic azides in dihydro[2H]pyrans

(Chemical Equation Presented) A synthesis of verdamicin C2 and its congener C2a has been accomplished from sisomicin relying on a novel oxidative transformation of an allylic azide to the corresponding α,β- unsaturated aldehyde, and its stereocontrolled elaboration into the intended 5′ side chain of verdamicin C2 and C2a. In vitro antibacterial testing shows that both C6′ epimers in verdamicin C2 and C2a are equally active against a variety of bacterial strains. Oxidation of allylic primary azides, ethers, and esters of 2-substituted dihydro[2H]pyrans with SeO2 leads directly to the corresponding aldehydes.

THE NITROGENATED ALLYLIC SYSTEM AS AN INTRAMOLECULAR NUCLEOPHILE: A NEW ROUTE TO PYRAZOLES

A new route to pyrazoles via the cyclization of N-allyl-N-nitrosoamides is described.

Obtention de composes ethyleniques difonctionnels par acetylation de cyclohexenes diversement substitues. Synthese d'esters d'acetyl cyclohexenyle

A series of 22 functionally substituted (i. e. ketone, nitrile, ester and alcohol) cycloalkenes was treated with a complex of acetic anhydride-zinc chloride.The influence exerted on the reaction by the function's nature and its position relative to the do