4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Indole-4-boronic acid pinacol ester
CAS: 388116-27-6
Molecular Formula: C14H18BNO2
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole - Names and Identifiers
| Name | Indole-4-boronic acid pinacol ester |
| Synonyms | Indole-4-boronic acid pin... 1H-indol-4-ylboronic acid pinacol Indole-4-boronic acid pinacol ester 1H-Indole-4-boronic acid, pinacol ester 4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-indole 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole 1H-Indole,4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, 2-(1H-Indol-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
| CAS | 388116-27-6 |
| InChI | InChI=1/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)11-6-5-7-12-10(11)8-9-16-12/h5-9,16H,1-4H3 |
| InChIKey | QDCIXBBEUHMLDN-UHFFFAOYSA-N |
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole - Physico-chemical Properties
| Molecular Formula | C14H18BNO2 |
| Molar Mass | 243.11 |
| Density | 1.11±0.1 g/cm3(Predicted) |
| Melting Point | 120-125°C(lit.) |
| Boling Point | 396.0±15.0 °C(Predicted) |
| Flash Point | 193.3°C |
| Vapor Presure | 4.03E-06mmHg at 25°C |
| pKa | 16.83±0.30(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.562 |
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R36 - Irritating to the eyes |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole - Introduction
Indole-4-boronic acid pinacol ester is an organic compound with the chemical formula C15H19BO2, it is a white solid.
The compound is commonly used as a boron reagent in metal organic chemical reactions. It is a useful reagent that can be developed as a starting point for the preparation of chemical drugs and other organic compounds. It can participate in a series of reactions, including Suzuki coupling reaction, reductive coupling reaction, nucleophilic addition reaction, etc.
The method for preparing Indole-4-boronic acid pinacol ester can be obtained by reacting 4-indole boronic acid and pinacol under appropriate reaction conditions. The specific synthesis method can refer to the literature of organic synthetic chemistry.
Regarding safety information, Indole-4-boronic acid pinacol ester is usually relatively safe under normal use conditions. However, the use of chemicals should follow appropriate practices and safe operating procedures. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated place. If you have any questions or unexpected situations, please consult a professional or refer to the safety data sheet of the chemical.
The compound is commonly used as a boron reagent in metal organic chemical reactions. It is a useful reagent that can be developed as a starting point for the preparation of chemical drugs and other organic compounds. It can participate in a series of reactions, including Suzuki coupling reaction, reductive coupling reaction, nucleophilic addition reaction, etc.
The method for preparing Indole-4-boronic acid pinacol ester can be obtained by reacting 4-indole boronic acid and pinacol under appropriate reaction conditions. The specific synthesis method can refer to the literature of organic synthetic chemistry.
Regarding safety information, Indole-4-boronic acid pinacol ester is usually relatively safe under normal use conditions. However, the use of chemicals should follow appropriate practices and safe operating procedures. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated place. If you have any questions or unexpected situations, please consult a professional or refer to the safety data sheet of the chemical.
Last Update：2024-04-09 20:45:29
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CAS: 388116-27-6
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CAS: 388116-27-6
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