(3-溴甲基苯基)硼酸频哪醇酯

(3-溴甲基苯基)硼酸频哪醇酯 - Names and Identifiers

Name	1,3,2-Dioxaborolane,2-[3-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-
Synonyms	(3-BROMOMETHYLPHENYL)BORONIC ACID PICOL ESTER (3-Bromomethylphenyl)Boronic Acid Pinacol Ester (3-BROMOMETHYLPHENYL)BORONIC ACID PINACOL ESTER 3-(Bromomethyl)benzeneboronic acid, pinacol ester 2-(3-(bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 2-[(3-broMoMethyl)phenyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolaMe 2-(3-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 1,3,2-Dioxaborolane,2-[3-(bromomethyl)phenyl]-4,4,5,5-tetramethyl- 3-(Bromomethyl)benzeneboronic acid pinacol ester 2-(3-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS	214360-74-4

(3-溴甲基苯基)硼酸频哪醇酯 - Physico-chemical Properties

Molecular Formula	C13H18BBrO2
Molar Mass	297
Density	1.26±0.1 g/cm3(Predicted)
Melting Point	89-91°C
Boling Point	360.9±25.0 °C(Predicted)
Flash Point	172.1 °C
Solubility	Chloroform (Slightly), Methanol (Slightly)
Appearance	powder
Color	white to off-white
Storage Condition	2-8°C

(3-溴甲基苯基)硼酸频哪醇酯 - Risk and Safety

Risk Codes	22 - Harmful if swallowed
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37 - Wear suitable gloves.
TSCA	No

(3-溴甲基苯基)硼酸频哪醇酯 - Introduction

1,3,2-Dioxaborolane,2-[3-(bromomethyl)phenyl]-4,4, 5,5-tetraethyl-(1,3,2-Dioxaborolane,2-[3-(bromomethyl)) phenyl]-4,4,5,5-tetramethyl-) is a compound. The following is a description of the properties, uses, preparation methods and safety information of the compound:

Nature:
-Appearance: colorless liquid
-Molecular formula: C15H19BO2Br
-Molecular weight: 304.13g/mol
-Melting point: No data
-Boiling Point: No data
-Solubility: Soluble in organic solvents such as chloroform, dichloromethane and ether

Use:
- 1,3,2-Dioxaborolane,2-[3-(bromomethyl)phenyl]-4,4, 5,5-tetraethyl-commonly used as a reagent in organic synthesis, carbon-carbon and carbon-boron bonds for the construction of compounds
-In transition metal-catalyzed reactions, the compound can participate in the reaction as a ligand

Method:
1,3,2-Dioxaborolane,2-[3-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-is generally synthesized by the following steps:
1. First, 2-(bromomethyl) benzyl alcohol and 2,3,4,5-tetramethylphenylborate are subjected to ketal reaction to obtain the target compound.

Safety Information:
-There is no detailed data on the safety of this compound, so it is necessary to follow the regular safety procedures of the laboratory when using it.
-Appropriate personal protective equipment, such as lab gloves and goggles, is required.
-Avoid contact with skin and eyes when handling, storing and handling this compound.
-Please ensure that you operate under fully ventilated laboratory conditions and avoid inhaling aerosols or vapors.

Last Update：2024-04-10 22:29:15