(1-phenylpropyl)Malonic acid diethyl ester
diethyl (1-phenylpropyl)propanedioate
CAS: 37556-02-8
Molecular Formula: C16H22O4
(1-phenylpropyl)Malonic acid diethyl ester - Names and Identifiers
| Name | diethyl (1-phenylpropyl)propanedioate |
| Synonyms | SC 197077 NSC 197077 Diethyl (1-phenylpropyl)malonate Diethyl 2-(1-phenylpropyl)Malonate diethyl (1-phenylpropyl)propanedioate diethyl 2-(1-phenylpropyl)propanedioate (1-phenylpropyl)Malonic acid diethyl ester Propanedioic acid, (1-phenylpropyl)-, diethyl ester |
| CAS | 37556-02-8 |
| InChI | InChI=1/C16H22O4/c1-4-13(12-10-8-7-9-11-12)14(15(17)19-5-2)16(18)20-6-3/h7-11,13-14H,4-6H2,1-3H3 |
(1-phenylpropyl)Malonic acid diethyl ester - Physico-chemical Properties
| Molecular Formula | C16H22O4 |
| Molar Mass | 278.34 |
| Density | 1.060 |
| Boling Point | 347℃ |
| Flash Point | 164℃ |
| Vapor Presure | 5.31E-05mmHg at 25°C |
| Refractive Index | 1.493 |
(1-phenylpropyl)Malonic acid diethyl ester - Introduction
diethyl (1-phenylpropyl)propanedioate is an organic compound with the chemical formula C18H24O4.
Nature:
diethyl (1-phenylpropyl)propanedioate is a colorless liquid and has a fragrance at room temperature. It is relatively soluble in terms of solubility and can be dissolved in most organic solvents.
Use:
diethyl (1-phenylpropyl)propanedioate is an important intermediate in organic synthesis. It can be used to synthesize other compounds, such as pharmaceuticals, spices and pesticides. In addition, it can also be used for synthetic polymer materials.
Preparation Method:
The preparation method of diethyl (1-phenylpropyl)propanedioate can be achieved by transesterification of styrene and diethyl malonate under appropriate conditions. This reaction requires the presence of a catalyst. Commonly used catalysts include triethyl sulfate or triethyl acetate. The specific operating conditions of the reaction can be adjusted according to actual needs.
Safety Information:
The use of diethyl (1-phenylpropyl)propanedioate should follow the appropriate safety procedures. It may be irritating to the eyes, skin and respiratory system. Therefore, it is necessary to wear suitable protective gloves, glasses and breathing apparatus to ensure a good ventilation environment. Avoid contact with strong oxidants and store in a dry, cool place. Chemical waste disposal regulations are to be observed when handling this material. In all cases, the relevant safety data sheets should be read and observed.
Nature:
diethyl (1-phenylpropyl)propanedioate is a colorless liquid and has a fragrance at room temperature. It is relatively soluble in terms of solubility and can be dissolved in most organic solvents.
Use:
diethyl (1-phenylpropyl)propanedioate is an important intermediate in organic synthesis. It can be used to synthesize other compounds, such as pharmaceuticals, spices and pesticides. In addition, it can also be used for synthetic polymer materials.
Preparation Method:
The preparation method of diethyl (1-phenylpropyl)propanedioate can be achieved by transesterification of styrene and diethyl malonate under appropriate conditions. This reaction requires the presence of a catalyst. Commonly used catalysts include triethyl sulfate or triethyl acetate. The specific operating conditions of the reaction can be adjusted according to actual needs.
Safety Information:
The use of diethyl (1-phenylpropyl)propanedioate should follow the appropriate safety procedures. It may be irritating to the eyes, skin and respiratory system. Therefore, it is necessary to wear suitable protective gloves, glasses and breathing apparatus to ensure a good ventilation environment. Avoid contact with strong oxidants and store in a dry, cool place. Chemical waste disposal regulations are to be observed when handling this material. In all cases, the relevant safety data sheets should be read and observed.
Last Update：2024-04-09 20:52:54
