86763-33-9

Basic information

• Product Name: S-(n-dodecyl) 4-methoxybenzothioate
• Synonyms: S-(n-dodecyl) 4-methoxybenzothioate
• CAS NO: 86763-33-9
• Molecular Weight: 336.539
• Mol File: 86763-33-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: S-(n-dodecyl) 4-methoxybenzothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(n-dodecyl) 4-methoxybenzothioate(86763-33-9)
• EPA Substance Registry System: S-(n-dodecyl) 4-methoxybenzothioate(86763-33-9)

Safety Data

• Hazardous Substances Data: 86763-33-9(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 112-55-0 1-dodecylthiol 
• 38117-54-3 cyclopentadienyl iron(II) dicarbonyl dimer 
• 696-62-8 para-iodoanisole 
• 201230-82-2 carbon monoxide 
• 26960-77-0 sodium dodecanethiolate 
• 1253793-77-9 O-(tert-butyl) S-dodecyl thiocarbonate 
• 66107-29-7 4-methoxyphenyl triflate 
• 150-76-5 4-methoxy-phenol 
• 20025-90-5 p-dodecylbenzenethiol 
• 100-07-2 4-methoxy-benzoyl chloride 
• 2757-37-1 didodecyl disulfide 

Downstream Products

• 123-11-5 4-methoxy-benzaldehyde 

Relevant articles and documents

Ni-Catalyzed Cross-Electrophile Coupling of Aryl Triflates with Thiocarbonates via C-O/C-O Bond Cleavage

A nickel-catalyzed reductive coupling of aryl triflates with thiocarbonates is reported here. Both electron-rich and -deficient aryl C(sp2)-O electrophiles as well as a class of O-tBu S-alkyl thiocarbonates are compatible with the optimized reaction conditions, as evidenced by 49 examples. The reaction also proceeds with good chemoselective cleavage of the C-O bond with regard to thioesters. This work broadens the scope of nickel-catalyzed reductive cross-electrophile coupling reactions.

Microwave-assisted Synthesis of Thioesters from Aldehydes and Thiols in Water

We describe the synthesis of thioesters via copper- or iron-catalyzed coupling of thiols with aldehydes on application of microwave irradiation. In this protocol, a variety of aliphatic and aromatic aldehydes and thiols were used, and the products were ob

Metal-free cross-coupling reaction of aldehydes with disulfides by using DTBP as an oxidant under solvent-free conditions

A DTBP-promoted C-H thiolation of aldehydes with disulfides under metal-free and solvent-free conditions is described. The system shows good functional group tolerance to afford thioesters in moderate to excellent yields. the Partner Organisations 2014.