3-Cyclohexene-1-carboxylic acid, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester
Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-cyclohexene-1-carboxylate
CAS: 1049004-32-1
Molecular Formula: C15H25BO4
3-Cyclohexene-1-carboxylic acid, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester - Names and Identifiers
3-Cyclohexene-1-carboxylic acid, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester - Physico-chemical Properties
| Molecular Formula | C15H25BO4 |
| Molar Mass | 280.17 |
| Density | 1.03 |
| Boling Point | 312.6±52.0 °C(Predicted) |
| Flash Point | 142.8±30.7 °C |
| Vapor Presure | 0.0±0.7 mmHg at 25°C |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Sensitive | Irritant |
| Refractive Index | 1.473 |
| MDL | MFCD11520546 |
3-Cyclohexene-1-carboxylic acid, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester - Introduction
1-Ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is also known as Boc-protected 4-cyclohexenone. The following is a description of its nature, use, preparation and safety information:
Nature:
1-Ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is a white solid with the property of being soluble in organic solvents. It is a stable compound that does not readily decompose under routine experimental conditions.
Use:
1-ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is commonly used as a protecting group in organic synthesis. It can protect the alcohol function to prevent unwanted side reactions in the reaction. In the synthesis, after the desired chemical reaction, the protecting group can be removed by appropriate conditions.
Preparation Method:
1-Ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester can be obtained by reacting 1-ethoxycyclohex-3-ene-4-one with 2,2-dimethyl -1,3-dioxolane boronic acid (ADB). The reaction is usually carried out at room temperature and under basic conditions.
Safety Information:
The safety of 1-ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is considered to be higher under general experimental conditions. However, for chemicals in chemical laboratories, it is important to follow proper laboratory practices and take appropriate safety measures. Chemicals should be stored in a cool, dry, well-ventilated place, away from fire and oxidizing agents.
Nature:
1-Ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is a white solid with the property of being soluble in organic solvents. It is a stable compound that does not readily decompose under routine experimental conditions.
Use:
1-ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is commonly used as a protecting group in organic synthesis. It can protect the alcohol function to prevent unwanted side reactions in the reaction. In the synthesis, after the desired chemical reaction, the protecting group can be removed by appropriate conditions.
Preparation Method:
1-Ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester can be obtained by reacting 1-ethoxycyclohex-3-ene-4-one with 2,2-dimethyl -1,3-dioxolane boronic acid (ADB). The reaction is usually carried out at room temperature and under basic conditions.
Safety Information:
The safety of 1-ethoxycarbonylcyclohex-3-ene-4-boronic acid pinacol ester is considered to be higher under general experimental conditions. However, for chemicals in chemical laboratories, it is important to follow proper laboratory practices and take appropriate safety measures. Chemicals should be stored in a cool, dry, well-ventilated place, away from fire and oxidizing agents.
Last Update：2024-04-09 20:45:29
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Product Name: Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate Visit Supplier Webpage Request for quotation
CAS: 1049004-32-1
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