7560-65-8

Basic information

• Product Name: 4-(Dimethoxymethyl)-1-cyclohexene
• Synonyms: 4-(Dimethoxymethyl)-1-cyclohexene;4-Dimethoxymethylcyclohexene;Cyclohexene, 4-(diMethoxyMethyl)-;4-(DiMethoxyMethyl)cyclohex-1-ene
• CAS NO: 7560-65-8
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.2221
• Mol File: 7560-65-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 179.8°Cat760mmHg
• Flash Point: 55.7°C
• Appearance: /
• Density: 0.949g/cm³
• Vapor Pressure: 1.25mmHg at 25°C
• Refractive Index: 1.454
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(Dimethoxymethyl)-1-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(Dimethoxymethyl)-1-cyclohexene(7560-65-8)
• EPA Substance Registry System: 4-(Dimethoxymethyl)-1-cyclohexene(7560-65-8)

Safety Data

• Hazardous Substances Data: 7560-65-8(Hazardous Substances Data)

Usage

General Description

4-(Dimethoxymethyl)-1-cyclohexene is a chemical compound with the molecular formula C9H16O2. It is a cycloalkene derivative with two methoxy groups and a methylene bridge attached to a cyclohexene ring. 4-(Dimethoxymethyl)-1-cyclohexene is commonly used in organic synthesis and as a building block for the production of various pharmaceuticals and fine chemicals. Its unique structure and reactivity make it a valuable intermediate for the synthesis of complex organic molecules. 4-(Dimethoxymethyl)-1-cyclohexene is also used as a reagent in the preparation of various heteroaromatic compounds and can be a valuable tool for chemists in the development of new materials and drug candidates.

InChI:InChI=1/C9H16O2/c1-10-9(11-2)8-6-4-3-5-7-8/h3-4,8-9H,5-7H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 85377-08-8 3-Aethoxy-4-hydroxy-benzaldehyd-dimethylacetal 
• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 2539-53-9 4-ethoxy-3-hydroxybenzaldehyde 
• 71118-99-5 3-butoxy-4-hydroxybenzaldehyde 
• 66488-78-6 4-butyloxy-3-hydroxybenzaldehyde 

Relevant articles and documents

A (3 - alkoxy - 4 - hydroxy) - cyclohexyl acetal glycol and its isomers of use

The present invention discloses a (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol, an (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol and synthesis methods and use therefor. The (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol and (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol can be used for synthesis of a variety of vanillin and iso-vanillin. Compared to the existing synthetic method, the synthesis method has simple steps, and less discharge of "three wastes".

Efficient acetalisation of aldehydes catalyzed by titanium tetrachloride in a basic medium

The acetalisation of aliphatic and aromatic aldehydes is achieved in a basic medium by using catalytic amount of Ti(IV) chloride in MeOH in the presence of NH3 or Et3N. The present protocol shows many advantages over the well known base or acid catalysis: in fact, in contrast to base-promoted acetalisation, aldehydes with electron-rich carbonyl groups react easily, enolizable aldehydes do not undergo aldol condensation and, in contrast to acid-catalysis, migration of the double bond does not occur in the preparation of α,β-unsaturated acetals.