Cyclohexanecarboxylic acid, 4,4-difluoro-, ethyl ester
ethyl 4,4-difluorocyclohexanecarboxylate
CAS: 178312-47-5
Molecular Formula: C9H14F2O2
Cyclohexanecarboxylic acid, 4,4-difluoro-, ethyl ester - Names and Identifiers
Cyclohexanecarboxylic acid, 4,4-difluoro-, ethyl ester - Physico-chemical Properties
| Molecular Formula | C9H14F2O2 |
| Molar Mass | 192.2 |
| Density | 1.10±0.1 g/cm3(Predicted) |
| Boling Point | 84-86°C/8mm |
| Flash Point | 84-86°C/8mm |
| Vapor Presure | 0.28mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.417 |
| MDL | MFCD03788494 |
Cyclohexanecarboxylic acid, 4,4-difluoro-, ethyl ester - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| Hazard Class | IRRITANT |
Cyclohexanecarboxylic acid, 4,4-difluoro-, ethyl ester - Introduction
ethyl 4, also known as ethyl-4, 4-difluorohexylbenzoate, is an organic compound. Its chemical formula is C10H13FO2.
Nature:
ethyl 4, is a colorless or yellowish solid that is flammable. It has low solubility and is almost insoluble in water. It can be dissolved in organic solvents such as alcohols and esters.
Use:
ethyl 4 can be used as a reagent in organic synthesis. It is often used as a catalyst in esterification reactions to promote the reaction of acids with alcohols to form esters. In addition, it can also be used in other organic synthesis reactions, such as etherification and acylation reactions.
Method:
ethyl 4, which can be obtained by reacting ethyl iodide with 4,4-difluorohexyl benzoic acid. The reaction is usually carried out in an organic solvent with the addition of a base catalyst.
Safety Information:
ethyl 4, is an organic compound, and attention should be paid to its safe operation. It is a combustible substance and should be kept away from open flames and high temperatures. When handling, wear appropriate protective measures such as gloves and safety glasses. Avoid direct contact with skin and eyes. If contact or inhalation occurs, rinse immediately with water or seek medical attention. When storing, it should be stored in a sealed container, away from open flames and high temperatures.
Nature:
ethyl 4, is a colorless or yellowish solid that is flammable. It has low solubility and is almost insoluble in water. It can be dissolved in organic solvents such as alcohols and esters.
Use:
ethyl 4 can be used as a reagent in organic synthesis. It is often used as a catalyst in esterification reactions to promote the reaction of acids with alcohols to form esters. In addition, it can also be used in other organic synthesis reactions, such as etherification and acylation reactions.
Method:
ethyl 4, which can be obtained by reacting ethyl iodide with 4,4-difluorohexyl benzoic acid. The reaction is usually carried out in an organic solvent with the addition of a base catalyst.
Safety Information:
ethyl 4, is an organic compound, and attention should be paid to its safe operation. It is a combustible substance and should be kept away from open flames and high temperatures. When handling, wear appropriate protective measures such as gloves and safety glasses. Avoid direct contact with skin and eyes. If contact or inhalation occurs, rinse immediately with water or seek medical attention. When storing, it should be stored in a sealed container, away from open flames and high temperatures.
Last Update：2024-04-10 22:29:15
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CAS: 178312-47-5
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