14395-53-0

Basic information

• Product Name: 2-BROMO-4-METHYL-BENZOTHIOL
• Synonyms: 2-BROMO-4-METHYL-BENZOTHIOL;2-Bromo-4-methylbenzyl thiol;2-Bromo-4-methylbenzenethiol
• CAS NO: 14395-53-0
• Molecular Formula: C₇H₇BrS
• Molecular Weight: 203.1
• Mol File: 14395-53-0.mol

Chemical Properties

• Boiling Point: 252.2°Cat760mmHg
• Flash Point: 106.3°C
• Appearance: /
• Density: 1.509g/cm³
• Vapor Pressure: 0.031mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: 2-BROMO-4-METHYL-BENZOTHIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-4-METHYL-BENZOTHIOL(14395-53-0)
• EPA Substance Registry System: 2-BROMO-4-METHYL-BENZOTHIOL(14395-53-0)

Safety Data

• Hazardous Substances Data: 14395-53-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-BROMO-4-METHYL-BENZOTHIOL is used as a key building block in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its unique chemical structure allows for the creation of a wide range of compounds with diverse therapeutic and pesticidal properties.
Used in Dye and Pigment Production:
In the dye and pigment industry, 2-BROMO-4-METHYL-BENZOTHIOL is utilized as an intermediate in the production of various dyes and pigments. Its chemical properties enable the synthesis of colorants with specific characteristics, such as brightness, stability, and solubility, which are essential for various applications in textiles, plastics, and printing inks.
Used in Organic Compound Preparation:
2-BROMO-4-METHYL-BENZOTHIOL also serves as an intermediate in the preparation of other organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of complex organic molecules, which can be used in various chemical and industrial processes.
Used in Corrosion Inhibition:
2-BROMO-4-METHYL-BENZOTHIOL has been studied for its potential use as a corrosion inhibitor in industrial applications. Its ability to form protective layers on metal surfaces can help prevent corrosion and extend the lifespan of equipment and structures in various industries, such as oil and gas, automotive, and construction.
However, it is crucial to handle 2-BROMO-4-METHYL-BENZOTHIOL with care, as it can be harmful if ingested, inhaled, or in contact with the skin, and may cause irritation to the respiratory system and eyes. Proper safety precautions, including the use of personal protective equipment and adherence to safety guidelines, should be taken when working with this compound.

InChI:InChI=1/C7H7BrS/c1-5-2-3-7(9)6(8)4-5/h2-4,9H,1H3

Upstream product

• 17067-13-9 (2-bromo-4-methyl-phenylsulfanyl)-acetic acid 
• 3996-29-0 2-[(4-methylphenyl)thio]acetic acid 
• 583-68-6 2-bromo-p-toluidine 

Downstream Products

• 17067-13-9 (2-bromo-4-methyl-phenylsulfanyl)-acetic acid 
• 92160-33-3 bis-(2-bromo-4-methyl-phenyl)-disulfide 
• 799763-97-6 2-(2-bromo-4-methylphenylsulfanyl)ethylamine 
• 799764-03-7 4-(2-bromo-4-methylphenylsulfanyl)butylamine 
• 799764-00-4 3-(2-bromo-4-methylphenylsulfanyl)propylamine 
• 944048-37-7 C₁₈H₁₆BrNOS 
• 946407-94-9 C₁₇H₁₃SO₂Br 
• 1609659-22-4 C₂₈H₃₉BN₂O₄S 
• 1620386-92-6 C₂₃H₃₁BN₂O₂S 
• 1609659-21-3 C₂₂H₂₇BrN₂O₂S 

Relevant articles and documents

An efficient synthesis of benzene fused six-, seven- and eight-membered rings containing nitrogen and sulfur by benzyne ring closure reaction

3,4-Dihydro-2-H-benzo[1,4]thiazines (3a-c), 2,3,4,5-tetrahydro[b]-[1,4] thiazapines (3d-f) and 2,3,4,5-tetrahydro-2H-benzo[b][1,4]thiazocines (3g-i) were prepared by the cyclization of the respective 2-bromophenylsulfanyl derivatives of ethylamine (1a-c), propylamine (2d-f) and butylamine (2g-i).