2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
1,3,2-Dioxaborolane, 2-[(3-chlorophenyl)methyl]-4,4,5,5-tetramethyl-
CAS: 517920-59-1
Molecular Formula: C13H18BClO2
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane - Names and Identifiers
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane - Physico-chemical Properties
| Molecular Formula | C13H18BClO2 |
| Molar Mass | 252.54 |
| Density | 1.08±0.1 g/cm3(Predicted) |
| Boling Point | 298.8±23.0 °C(Predicted) |
| Storage Condition | 2-8°C |
| MDL | MFCD10698516 |
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane - Introduction
1,3,2-Dioxaborolane, 2-[(3-chlorophyll) methyl]-4,4, 5,5-tetraethyl-is an organic compound with the chemical formula C13H18BClO2, which is a colorless liquid.
The compound has the following properties:
-Melting point:-15°C
-Boiling point: 220°C
-Stability: stable at room temperature, but will gradually decompose in the sun
-Solubility: Soluble in organic solvents such as ether, dimethyl ketone and benzene
The main use of 1,3,2-Dioxaborolane, 2-[(3-chlorophyll) methyl]-4,4, 5,5-tetraethyl-is as a reagent in organic synthesis. It can be used as a boron reagent and as a catalyst for cross-coupling reactions.
The method for preparing 1,3,2-Dioxaborolane, 2-[(3-chlorophyll) methyl]-4,4, 5,5-tetraethyl-is as follows:
First, p-chlorobenzaldehyde and 1,1, 1-trimethylethylboronic anhydride are reacted to generate 2-[(3-chlorophenyl) methyl]-4,4, 5,5-tetramethyl -1,3, 2-dioxoborovaleric acid. The acid is then reacted with an excess of trimethylamine to give the target compound.
With regard to safety information, there is currently no detailed report on the specific toxicity and harmfulness of this compound. Therefore, general laboratory safety practices should be followed during use and operated in a well-ventilated area. In case of skin contact or swallowing, seek medical attention immediately.
The compound has the following properties:
-Melting point:-15°C
-Boiling point: 220°C
-Stability: stable at room temperature, but will gradually decompose in the sun
-Solubility: Soluble in organic solvents such as ether, dimethyl ketone and benzene
The main use of 1,3,2-Dioxaborolane, 2-[(3-chlorophyll) methyl]-4,4, 5,5-tetraethyl-is as a reagent in organic synthesis. It can be used as a boron reagent and as a catalyst for cross-coupling reactions.
The method for preparing 1,3,2-Dioxaborolane, 2-[(3-chlorophyll) methyl]-4,4, 5,5-tetraethyl-is as follows:
First, p-chlorobenzaldehyde and 1,1, 1-trimethylethylboronic anhydride are reacted to generate 2-[(3-chlorophenyl) methyl]-4,4, 5,5-tetramethyl -1,3, 2-dioxoborovaleric acid. The acid is then reacted with an excess of trimethylamine to give the target compound.
With regard to safety information, there is currently no detailed report on the specific toxicity and harmfulness of this compound. Therefore, general laboratory safety practices should be followed during use and operated in a well-ventilated area. In case of skin contact or swallowing, seek medical attention immediately.
Last Update：2024-04-10 22:29:15
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