Others
Reliable factory customized supply 2-(2,4-dimethyl-3-cyclohexen-1-yl)-1,3-dioxolane 67893-07-6
- 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)
-
67893-07-6 Process route
-
-
3984-22-3
2-vinyl-1,3-dioxolane
-
-
926-54-5
trans-2-methyl-1,3-pentadiene
-
-
67893-07-6
2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane
| Conditions | Yield |
|---|---|
|
|
58%
|
-
-
68039-49-6
2,4-dimethyl-3-cyclohexenecarboxaldehyde
-
-
107-21-1
ethylene glycol
-
-
67893-07-6
2'-(2,6-dimethyl-3-cyclohexenyl)-1,3-dioxolane
| Conditions | Yield |
|---|---|
|
With
1-hexyl-3-methylimidazolium tetrafluoroborate;
at 130 ℃;
for 3h;
|
67893-07-6 Upstream products
-
3984-22-3
2-vinyl-1,3-dioxolane
-
926-54-5
trans-2-methyl-1,3-pentadiene
-
68039-49-6
2,4-dimethyl-3-cyclohexenecarboxaldehyde
-
107-21-1
ethylene glycol
RELATED PRODUCTS