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2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane

  • CAS No.: 67893-07-6
  • Purity: 99%
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  • Molecular Formula: C11H18O2
  • Molecular Weight: 182.263
  • Vapor Pressure: 0.0533mmHg at 25°C 
  • Boiling Point: 242.3°C at 760 mmHg 
  • Flash Point: 101.6°C 
  • PSA: 18.46000 
  • Density: 1g/cm3 
  • LogP: 2.35170 

2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane(Cas 67893-07-6) Usage

Chemical structure

2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane consists of a dioxolane ring with a cyclohexene group attached to it.

Physical properties

It is a colorless liquid with a sweet, floral odor.

Usage

It is commonly used as a flavoring agent in the food and beverage industry, and as a fragrance ingredient in cosmetic and personal care products.

Synthesis

It is synthesized through the reaction of 2,4-dimethyl-cyclohex-2-en-1-one with ethylene glycol in the presence of an acid catalyst.

Safety

It may have potential health hazards if not used properly and it is important to handle 2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane with care.

General Description

2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane is a chemical compound that consists of a dioxolane ring with a cyclohexene group attached to it. It is a colorless liquid with a sweet, floral odor, and it is commonly used as a flavoring agent in the food and beverage industry. It is also used as a fragrance ingredient in cosmetic and personal care products. 2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane is synthesized through the reaction of 2,4-dimethyl-cyclohex-2-en-1-one with ethylene glycol in the presence of an acid catalyst. It is important to handle this compound with care as it may have potential health hazards if not used properly.

InChI:InChI=1/C11H18O2/c1-8-3-4-10(9(2)7-8)11-12-5-6-13-11/h7,9-11H,3-6H2,1-2H3

67893-07-6 Relevant articles

Non-acid catalytic acetalisation of aldehydes with diols in ionic liquids

Zhang, Fan,Xu, Dan-Qian,Luo, Shu-Ping,Liu, Bao-You,Du, Xiao-Hua,Xu, Zhen-Yuan

, p. 773 - 774 (2007/10/03)

The acetalisation of aldehydes with diol...

Acrolein Acetals as Allyl Cation Precursors in the Ionic Diels-Alder Reaction

Gassman, Paul G.,Singleton, Daniel A.,Wilwerding, James J.,Chavan, Subhash P.

, p. 2182 - 2184 (2007/10/02)

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67893-07-6 Process route

2-vinyl-1,3-dioxolane
3984-22-3

2-vinyl-1,3-dioxolane

trans-2-methyl-1,3-pentadiene
926-54-5

trans-2-methyl-1,3-pentadiene

2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane
67893-07-6

2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane

Conditions
Conditions Yield
58%
2,4-dimethyl-3-cyclohexenecarboxaldehyde
68039-49-6

2,4-dimethyl-3-cyclohexenecarboxaldehyde

ethylene glycol
107-21-1

ethylene glycol

2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane
67893-07-6

2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane

Conditions
Conditions Yield
With 1-hexyl-3-methylimidazolium tetrafluoroborate; at 130 ℃; for 3h;

67893-07-6 Upstream products

  • 3984-22-3
    3984-22-3

    2-vinyl-1,3-dioxolane

  • 926-54-5
    926-54-5

    trans-2-methyl-1,3-pentadiene

  • 68039-49-6
    68039-49-6

    2,4-dimethyl-3-cyclohexenecarboxaldehyde

  • 107-21-1
    107-21-1

    ethylene glycol

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