710348-63-3

710348-63-3 - Names and Identifiers

Name	(2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid
Synonyms	3-(METHYLTHIO)PHENYLBORONIC ACID PINACOLATE 3-METHYLTHIOPHENYLBORONIC ACID, PINACOL ESTER 3-3-(Methylthio)phenylboronic acid pinacolate 3-(Methylthio)phenylboronic acid pinacol ester 3-(METHYLTHIO)PHENYLBORONIC ACID PINACOL ESTER 2-(3-Methylthiophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)... 4,4,5,5-tetramethyl-2-(3-(methylthio)phenyl)-1,3,2-dioxaborolane 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[3-(methylthio)phenyl]- (2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid
CAS	710348-63-3
InChI	InChI=1/C13H21BO3S/c1-12(2,15)13(3,4)17-14(16)10-7-6-8-11(9-10)18-5/h6-9,15-16H,1-5H3

710348-63-3 - Physico-chemical Properties

Molecular Formula	C13H19BO2S
Molar Mass	250.16
Density	1.06g/ml
Boling Point	392.681°C at 760 mmHg
Flash Point	191.287°C
Vapor Presure	0mmHg at 25°C
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.534

710348-63-3 - Risk and Safety

Hazard Class

IRRITANT

710348-63-3 - Introduction

(2-hydroxy-1, 1,2-trimethy1-propoxy)-(3-methylsulfanylphenyl)borinic acid, the chemical name is ((2-hydroxy-1, 1,2-trimethylpropoxy)-(3-methylthiophenyl) boronic acid), is an organic boron compound. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: usually white crystal or solid powder
-Melting point: about 95-105 degrees Celsius
-Molecular formula: C12H19BO3S
-Molecular weight: 256.19g/mol
-Solubility: Good solubility in many organic solvents

Use:
(2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid is a commonly used organic boron reagent, which has a wide range of applications in synthetic chemistry:
-Used as coupling reagent: It can carry out boronic acid coupling reaction with functional groups such as alcohol, phenol and amine to form C- B bonds. This reaction is very useful for building carbon-boron bonds.
-Used as a catalyst: It can be used as a catalyst for some organic reactions, such as asymmetric transfer hydrogenation.

Preparation Method:
(2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid can be obtained by heating reaction of phenylboronic acid with 2-bromo-2-methyl-1-benzenethiol propane in ethanol.

Safety Information:
-Data on toxicity and danger to humans are limited, but caution should be exercised.
-Avoid contact with skin and eyes, and avoid inhaling its dust.
-Wear suitable personal protective equipment such as lab gloves, goggles and protective masks during operation.
-should be in a well ventilated place to operate, avoid inhalation of volatile gas or dust.
-During storage and handling, the relevant safety regulations and operating procedures should be observed.

Please read the relevant safety data sheet and operation manual carefully before use, and consult professional advice.

Last Update：2024-04-10 22:29:15