18906-37-1

Basic information

• Product Name: 2,4-dimethoxybenzene-1-thiol
• Synonyms: 2,4-dimethoxybenzene-1-thiol;2,4-dimethoxybenzenethiol
• CAS NO: 18906-37-1
• Molecular Formula: C₈H₁₀O₂S
• Molecular Weight: 170.231
• Mol File: 18906-37-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 278.1 °C at 760 mmHg
• Flash Point: 122 °C
• Appearance: /
• Density: 1.134 g/cm³
• Vapor Pressure: 0.00734mmHg at 25°C
• Refractive Index: 1.549
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,4-dimethoxybenzene-1-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dimethoxybenzene-1-thiol(18906-37-1)
• EPA Substance Registry System: 2,4-dimethoxybenzene-1-thiol(18906-37-1)

Safety Data

• Hazardous Substances Data: 18906-37-1(Hazardous Substances Data)

Usage

Description

2,4-Dimethoxybenzene-1-thiol is a phenolic derivative characterized by the presence of two methoxy groups at the 2nd and 4th positions on the benzene ring and a thiol (-SH) group at the 1st position. This organic compound is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
2,4-Dimethoxybenzene-1-thiol is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to serve as a building block in the development of new pharmaceutical compounds, contributing to the advancement of medical treatments.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2,4-dimethoxybenzene-1-thiol is utilized as a versatile intermediate for the production of a wide range of organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of various chemicals, including dyes, agrochemicals, and other specialty chemicals.
Used in Research and Development:
2,4-Dimethoxybenzene-1-thiol is also employed in research and development settings, where it is used to study the properties and behavior of thiol-containing compounds. Its unique structure allows scientists to explore new reaction pathways and develop innovative synthetic methods, further expanding the potential applications of this compound.

Physical state

2,4-dimethoxybenzene-1-thiol is a Low-Melting Solid.

InChI:InChI=1/C8H10O2S/c1-9-6-3-4-8(11)7(5-6)10-2/h3-5,11H,1-2H3

Upstream product

• 151-10-0 1,3-Dimethoxybenzene 
• 571167-30-1 3-(2,4-dimethoxyphenyl)-sulfanyl-propionic acid methyl ester 
• 160855-21-0 N-(2,4-dimethoxyphenylthio)phthalimide 
• 63624-28-2 2,4-dimethoxybenzenesulfonylchloride 
• 2735-04-8 2,4-Dimethoxyaniline 

Downstream Products

• 5633-61-4 2,4-dimethoxy-1-(methylsulfanyl)benzene 
• 21552-25-0 [2,5-Dichloro-4-(2,4-dimethoxy-phenylsulfanylthiocarbonylamino)-phenyl]-dithiocarbamic acid 2,4-dimethoxy-phenyl ester 
• 55990-92-6 1,2-bis(2,4-dimethoxyphenyl)disulfane 
• 127905-84-4 [2-(2,4-Dimethoxy-phenylsulfanyl)-benzyl]-methyl-amine 
• 127905-75-3 N,N-dimethyl-2-(2,4-dimethoxyphenylthio)benzylamine 
• 127905-95-7 2-(2,4-Dimethoxy-phenylsulfanyl)-benzylamine 
• 127906-20-1 AE-641/30109032 
• 127906-35-8 4-(2-Methylaminomethyl-phenylsulfanyl)-benzene-1,3-diol 
• 127905-57-1 2-(2,4-Dimethoxy-phenylsulfanyl)-N,N-dimethyl-benzamide 
• 127905-52-6 2-(2,4-Dimethoxy-phenylsulfanyl)-N-methyl-benzamide 
• 127905-42-4 2-(2,4-Dimethoxy-phenylsulfanyl)-benzoyl chloride 
• 127905-46-8 2-(2,4-Dimethoxy-phenylsulfanyl)-benzamide 
• 127905-34-4 2-(2,4-Dimethoxyphenylthio)benzoic acid 
• 1379354-68-3 thioacetic acid S-(2,4-dimethoxy-phenyl ester) 

Relevant articles and documents

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Phthalimidesulfenyl chloride. x1. a synthetic equivalent of hs+ and+s-s+ species in electrophilic aromatic substitutions

The reaction of phthalimidesulfenyl chloride, 1, with activated arenes provides monosubstituted phthalimidesulfenyl derivatives 3 which can be easily transformed into the corresponding disulfides 7, thiols 8 and masked thiols 9.