260415-85-8
3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone
CAS: 260415-85-8
Molecular Formula: C18H26O4
260415-85-8 - Names and Identifiers
260415-85-8 - Physico-chemical Properties
| Molecular Formula | C18H26O4 |
| Molar Mass | 306.4 |
260415-85-8 - Introduction
3-(5,5-dimethy-1, 3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone is an organic compound. The following is an introduction to its nature, use, preparation and safety information.
Nature:
-Appearance: A colorless to pale yellow liquid.
-Molecular formula: C16H24O3
-Molecular weight: 264.36g/mol
-Melting point:-10 ℃
-Boiling point: 223-225 ℃
-Density: 0.99g/cm³
Use:
- 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone is commonly used as an ingredient in flavors and fragrances.
-It can also be used to synthesize other organic compounds.
Method:
3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone is prepared as follows:
1. 4-ethoxybenzaldehyde and 5,5-dimethyl -1,3-dioxane react under alkaline conditions to generate the corresponding alcohol compound.
2. The alkylation reaction is carried out by reacting the alcohol compound with bromobutane under alkaline conditions.
3. Finally, The alkylation reaction is used to convert the alkyl compound into the target product.
Safety Information:
-During operation, you need to avoid contact with skin and eyes.
- 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone may be toxic to aquatic organisms and should be avoided to cause environmental pollution.
-When storing and using, please follow the correct safe operation method.
Nature:
-Appearance: A colorless to pale yellow liquid.
-Molecular formula: C16H24O3
-Molecular weight: 264.36g/mol
-Melting point:-10 ℃
-Boiling point: 223-225 ℃
-Density: 0.99g/cm³
Use:
- 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone is commonly used as an ingredient in flavors and fragrances.
-It can also be used to synthesize other organic compounds.
Method:
3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone is prepared as follows:
1. 4-ethoxybenzaldehyde and 5,5-dimethyl -1,3-dioxane react under alkaline conditions to generate the corresponding alcohol compound.
2. The alkylation reaction is carried out by reacting the alcohol compound with bromobutane under alkaline conditions.
3. Finally, The alkylation reaction is used to convert the alkyl compound into the target product.
Safety Information:
-During operation, you need to avoid contact with skin and eyes.
- 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-ethoxyphenyl)-1-Butanone may be toxic to aquatic organisms and should be avoided to cause environmental pollution.
-When storing and using, please follow the correct safe operation method.
Last Update：2024-04-10 22:29:15
