38630-01-2

Basic information

• Product Name: (2,6-dimethylphenyl)(o-tolyl)sulfane
• Synonyms: (2,6-dimethylphenyl)(o-tolyl)sulfane
• CAS NO: 38630-01-2
• Molecular Weight: 228.358
• Mol File: 38630-01-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2,6-dimethylphenyl)(o-tolyl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: (2,6-dimethylphenyl)(o-tolyl)sulfane(38630-01-2)
• EPA Substance Registry System: (2,6-dimethylphenyl)(o-tolyl)sulfane(38630-01-2)

Safety Data

• Hazardous Substances Data: 38630-01-2(Hazardous Substances Data)

Upstream product

• 118-72-9 2,6-dimethylbenzene-1-thiol 
• 615-37-2 ortho-methylphenyl iodide 
• 6781-98-2 2,6-dimethyl-1-chlorobenzene 
• 137-06-4 2-thiocresol 
• 576-22-7 2-Bromo-m-xylene 
• 34878-60-9 sodium o-thiocresolate 
• 34878-61-0 sodium 2,6-dimethylphenylthiolate 

Downstream Products

• 103272-90-8 (2-Methyl-phenyl)-(2,6-dimethyl-phenyl)-sulfon 

Relevant articles and documents

Carbon-sulfur bond formation of challenging substrates at low temperature by using Pd-PEPPSI-IPent

Aryl thiols made cool and quick: The coupling of alkyl, aryl, and silyl thiols to hindered, deactivated aryl bromides and chlorides has been achieved under the most mild temperatures yet reported (i.e., room temperature to 40°C). The bulk afforded by the di-2,6-(3-propylphenyl)imidazolium-derived Pd-PEPPSI-IPent catalyst is believed to actively promote the critical reductive elimination step of the catalytic cycle, thereby eliminating the formation of poisonous off-cycle dimeric resting states that have plagued Pd-catalyzed sulfination reactions.

Ultraviolet spectra of diphenyl sulphides, polyphenylene sulphides and polyphenylene ethers

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