28046-69-7

Usage

Type of compound

Cyclic ether

Functional groups

Two methoxy groups

Position of methoxy groups

Attached to the 1 and 4 positions of the cyclohexane ring

Usage

Solvent in organic synthesis and fragrance in the perfume industry

Odor

Mild, sweet, floral

Stability

Relatively stable under normal conditions

Toxicity

Low toxicity

Environmental impact

Not known to be harmful to the environment when used in appropriate quantities

Safety precautions

Should be handled with care and proper safety precautions should be taken when working with it.

Upstream product

• 6995-79-5 cyclohexane-1,4-diol 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 1165952-92-0 cyclohexa-1,4-diene 
• 100314-09-8 trans-N_.N'-Dinitroso-N_.N'-dicarbethoxy-1.4-diamino-cyclohexan 
• 124-41-4 sodium methylate 

Relevant academic research and scientific papers

Syntheses and conformational analyses of mono- and trans-1,4-dialkoxy substituted cyclohexanes-the steric substituent/skeleton interactions

Mono- and trans-1,4-dialkoxy substituted cyclohexanes (alkyl=Me, Et, i-Pr, t-Bu) were prepared using the solvomercuration-demercuration (SM-DM) procedure. The axial?axial and axial,axial?equatorial, equatorial conformational equilibria of the products wer

Three Component Reactions. XX. Methoxymercuration of Cyclohexa-1,4-dienes

The methoxymercuration of several cyclohexa-1,4-dienes leads to insoluble mixtures of mono- and bismercuricompounds 2-4 and 5-7.After reduction with NaBH4/NaOH mixtures of methoxycyclohexenes and bismethoxycyclohexanes result.The result of capillary gaschromatographic analyses and n.m.r. spectra allows a semiquantitative evaluation of the reaction pathways.