2570-45-8

Basic information

• Product Name: 1,3-DIMETHOXY-5-METHYLTHIOBENZENE
• Synonyms: 1,3-DIMETHOXY-5-METHYLTHIOBENZENE
• CAS NO: 2570-45-8
• Molecular Formula: C₉H₁₂O₂S
• Molecular Weight: 184.25538
• Mol File: 2570-45-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 277.4°C at 760 mmHg
• Flash Point: 121.5°C
• Appearance: /
• Density: 1.11g/cm³
• Vapor Pressure: 0.00766mmHg at 25°C
• Refractive Index: 1.543
• CAS DataBase Reference: 1,3-DIMETHOXY-5-METHYLTHIOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIMETHOXY-5-METHYLTHIOBENZENE(2570-45-8)
• EPA Substance Registry System: 1,3-DIMETHOXY-5-METHYLTHIOBENZENE(2570-45-8)

Safety Data

• Hazardous Substances Data: 2570-45-8(Hazardous Substances Data)

Usage

Aromatic Properties

Known for its aromatic properties, which contribute to its use in fragrances and flavoring agents.

Physical State

Colorless to pale yellow liquid

Fragrances

Used in the production of fragrances due to its aromatic properties.

Organic Synthesis

Acts as a building block in organic synthesis.

Flavoring Agent

Used in some food and beverage products as a flavoring agent.

Toxicity

Can be toxic if ingested or inhaled.

Skin and Eye Irritation

May cause irritation to the skin and eyes.

Handling

Appropriate safety measures should be taken when handling this chemical to minimize risks.

InChI:InChI=1/C9H12O2S/c1-10-7-4-8(11-2)6-9(5-7)12-3/h4-6H,1-3H3

Upstream product

• 2432-51-1 ethylthioacetic acid methyl ester 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 5271-38-5 2-methylmercapto-ethanol 
• 25245-27-6 1-iodo-3,5-dimethoxybenzene 
• 624-92-0 Dimethyldisulphide 
• 38452-17-4 1,3-dimethoxy-5-(methylsulfinyl)benzene 
• 54839-87-1 O-(3,5-dimethoxyphenyl)dimethyl thiocarbamate 
• 500-99-2 3,5-dimethoxyphenol 
• 19689-66-8 3,5-dimethoxybenzenethiol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 19179-31-8 3,5-dimethoxy-benzonitrile 
• 100-68-5 methyl-phenyl-thioether 
• 849919-97-7 1-(2,6-dimethoxy-4-methylthiophenyl)-2-nitropropene 
• 849919-95-5 2,6-dimethoxy-4-methylthiobenzaldehyde 
• 54839-91-7 5-methylsulfanyl-resorcinol 
• 38452-46-9 1-Methanesulfonyl-3,5-dimethoxy-benzene 
• 38452-17-4 1,3-dimethoxy-5-(methylsulfinyl)benzene 

Relevant articles and documents

Nickel-Catalyzed Reversible Functional Group Metathesis between Aryl Nitriles and Aryl Thioethers

We describe a new functional group metathesis between aryl nitriles and aryl thioethers. The catalytic system nickel/dcype is essential to achieve this fully reversible transformation in good to excellent yields. Furthermore, the cyanide- and thiol-free reaction shows high functional group tolerance and great efficiency for the late-stage derivatization of commercial molecules. Finally, synthetic applications demonstrate its versatility and utility in multistep synthesis.

Construction of Biaryls from Aryl Sulfoxides and Anilines by Means of a Sigmatropic Rearrangement

An unprecedented S?N variant of the benzidine rearrangement for construction of biaryls has been developed. Aryl sulfoxides underwent dehydrogenative coupling with anilines by successive treatment with trifluoromethanesulfonic anhydride and trifluorometha