M4476G1

M4476G1 - Names and Identifiers

Name	[2-(methylsulfinyl)phenyl]boronic acid
Synonyms	M4476G1 1-Borono-2-(methylsulphinyl)benzene 2-(Methylsulphonyl)phenylboronicacid 2-(METHYLSULFINYL)PHENYLBORONIC ACID (2-Methanesulfinylphenyl)boronic acid 2-(METHYLSULPHINYL)BENZENEBORONIC ACID [2-(methylsulfinyl)phenyl]boronic acid Boronic acid, B-[2-(methylsulfinyl)phenyl]-
CAS	850567-97-4
InChI	InChI=1/C7H9BO3S/c1-12(11)7-5-3-2-4-6(7)8(9)10/h2-5,9-10H,1H3

M4476G1 - Physico-chemical Properties

Molecular Formula	C7H9BO3S
Molar Mass	184.02
Density	1.37±0.1 g/cm3(Predicted)
Melting Point	118-122°C
Boling Point	440.5±47.0 °C(Predicted)
Flash Point	220.2°C
Water Solubility	Slightly soluble in water.
Vapor Presure	1.55E-08mmHg at 25°C
pKa	8.46±0.58(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.616

M4476G1 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
HS Code	29319090
Hazard Class	IRRITANT

M4476G1 - Introduction

[2-(methylsulfinyl)phenyl]boronic acid is an organic compound with the chemical formula C7H9BO4S. Its main properties are as follows:

1. Appearance: [2-(methylsulfinyl)phenyl]boronic acid is a white solid.

2. Solubility: It is soluble in many organic solvents, such as methanol and dichloromethane.

3. stability:[2-(methylsulfinyl)phenyl]boronic acid is stable and can be stored for a long time at room temperature.

4. use:[2-(methylsulfinyl)phenyl]boronic acid is an important organic synthesis intermediates, commonly used in the synthesis of aldehydes and ketones. It can be used as a precursor of borane to generate disubstituted phenyl boron alcohols through the reaction of the method, and then participate in the coupling reaction to synthesize new compounds.

5. Preparation method:[2-(methylsulfinyl)phenyl]boronic acid can be prepared by direct thionation of phenylboronic acid. First, under the reaction conditions of phenylboronic acid and sulfurous acid, sulfurous acid will react with phenylboronic acid to form an intermediate sulfite. Subsequently, by heating and treatment with acetonitrile, [2-(methylsulfinyl)phenyl]boronic acid was generated.

6. safety information:[2-(methylsulfinyl)phenyl]boronic acid has no obvious toxicity or irritation to human body under general operating conditions. However, during the operation, appropriate protective measures should be taken, such as wearing protective glasses and gloves, to avoid direct contact with skin and eyes. In addition, care should be taken to avoid inhalation or ingestion. During storage, it should be kept in a dry, cool place, away from fire and oxidizing agents.

Last Update：2024-04-10 22:29:15