27826-43-3

Basic information

• Product Name: n-butyl(4-nitrophenyl) sulfane
• Synonyms: n-butyl(4-nitrophenyl) sulfane
• CAS NO: 27826-43-3
• Molecular Formula: C₁₀H₁₃NO₂S
• Molecular Weight: 211.28
• Mol File: 27826-43-3.mol
• Article Data: 21

Chemical Properties

• Appearance: /
• CAS DataBase Reference: n-butyl(4-nitrophenyl) sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: n-butyl(4-nitrophenyl) sulfane(27826-43-3)
• EPA Substance Registry System: n-butyl(4-nitrophenyl) sulfane(27826-43-3)

Safety Data

• Hazardous Substances Data: 27826-43-3(Hazardous Substances Data)

Upstream product

• 109-69-3 n-Butyl chloride 
• 45797-13-5 4-nitrophenylthiolate 
• 109-65-9 1-bromo-butane 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 629-45-8 dibutyl disulfide 
• 100-00-5 4-chlorobenzonitrile 
• 109-79-5 n-butanethiol 
• 17763-80-3 para-nitrophenyl triflate 
• 1849-36-1 para-nitrobenzenethiol 
• 542-69-8 1-iodo-butane 
• 201230-82-2 carbon monoxide 
• 636-98-6 p-nitrobenzene iodide 
• 586-78-7 para-nitrophenyl bromide 
• 4269-98-1 butanethiol thiouronium hydrobromide 

Downstream Products

• 78597-96-3 4-butylsulfonylnitrobenzene 
• 76410-92-9 1-(butylsulfinyl)-4-nitrobenzene 
• 92286-68-5 4-butylsulfanyl-aniline; hydrochloride 
• 51770-72-0 (4-Aminophenyl)-butyl-sulfon 
• 836-30-6 4-ntrophenyl(phenyl)amine 

Relevant articles and documents

Exploration of the mechanism and scope of the CuI/DABCO catalysed C–S coupling reaction

A cost effective and easily available CuI/DABCO catalytic system has been developed for the C–S cross-coupling reaction. This method is extremely useful for the thioetherification of aryl and heteroaryl halides, providing excellent yields and good chemoselectivity. We have also explored the mechanism of the reaction using DFT studies.

C-S cross-coupling of aryl halides with alkyl thiols catalyzed by in-situ generated nickel(II) N-heterocyclic carbene complexes

The C-S cross-coupling of aryl halides with alkyl thiols catalyzed by in-situ generated Ni (II) N-heterocyclic carbene (NHC) complexes is investigated. Good to excellent yields can be obtained for a variety of aryl halides when using 5 mol% of the Ni (II)-NHC catalyst and 1.5 eq. of KOtBu. Both the electronic and steric effects of the NHC ligands on the catalytic performance of Ni (II)-NHC, as well as the electronic effects of aryl halides on coupling reactivity are examined. The mechanism for Ni (II)-NHC catalyzed coupling reactions is also discussed.

Iridium and phosphine promoted C-F bond activation: The C-S cross-coupling of aryl fluorides with diaryl disulfides to synthesize thioethers

Carbon-fluorine bond is the strongest known single bond to carbon and proved very difficult to cleave. An iridium and phosphine promoted C-F bond activation was developed, for the first time achieving the C-S cross-coupling reaction of disulfides with aryl fluorides using iridium complex. The corresponding monoarylthiolation products were obtained at moderate to good yields. Thus, it represents a new method for the synthesis of aryl sulfides through C-F bond activation.