21101-60-0

Basic information

• Product Name: Phenol, 4-[(4-nitrophenyl)thio]-
• CAS NO: 21101-60-0
• Molecular Formula: C12H9NO3S
• Molecular Weight: 247.274
• Mol File: 21101-60-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Phenol, 4-[(4-nitrophenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[(4-nitrophenyl)thio]-(21101-60-0)
• EPA Substance Registry System: Phenol, 4-[(4-nitrophenyl)thio]-(21101-60-0)

Safety Data

• Hazardous Substances Data: 21101-60-0(Hazardous Substances Data)

Upstream product

• 937-32-6 4-nitrobenzenesulfenyl chloride 
• 108-95-2 phenol 
• 637-89-8 4-sulfanylphenol 
• 586-78-7 para-nitrophenyl bromide 
• 636-98-6 p-nitrobenzene iodide 
• 17796-89-3 1-[(4-nitrophenyl)sulfanyl]pyrrolidine-2,5-dione 
• 27691-43-6 1-(benzylsulphanyl)-4-Nitrobenzene 
• 1849-36-1 para-nitrobenzenethiol 
• 701-57-5 1-methylthio-4-nitro-benzene 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 62-53-3 aniline 
• 101-59-7 4-amino-4'-nitrodiphenyl sulfide 
• 110-46-3 isopentyl nitrite 
• 350-46-9 4-Fluoronitrobenzene 

Downstream Products

• 1241-12-9 4-(2-Diethylaminoethoxy-4'-nitrodiphenyl Sulfide 
• 100062-94-0 4-(4-aminophenylsulfamyl)phenol 
• 62248-53-7 4-(4-ethoxy-phenylsulfanyl)-aniline 
• 62248-51-5 4-(4-butoxyphenyl)thioaniline 
• 1375738-29-6 4-benzyloxy-4'-nitrodiphenylsulfide 
• 62248-47-9 4-butoxy-4'-nitrodiphenylsulfide 
• 876486-96-3 4-ethoxy-4'-nitrodiphenylsulfide 
• 1375738-26-3 4-propoxy-4'-nitrodiphenylsulfide 
• 59010-91-2 O-Methyl O-[4-(4'-nitrophenylthio)phenyl] S-n-propyl Phosphorothiolate 

Relevant articles and documents

Making the family portrait complete: Synthesis of Electron Withdrawing Group activated Hoveyda-Grubbs catalysts bearing sulfone and ketone functionalities

Synthesis of five Electron Withdrawing Group (EWG) activated Hoveyda-Grubbs’ catalysts containing thioperfluoroalkyl, sulfone and ketone functions is reported. The catalytic activity of these catalysts was well correlated with the σp values of

TBATB mediated debenzylative cross-coupling of aryl benzyl sulfides with electron rich compounds: Synthesis of diaryl sulfides

An efficient TBATB mediated debenzylative cross coupling of aryl benzyl sulfides with electron rich compounds provides diaryl sulfides in moderate to excellent yield. The salient features of the present protocol are simplicity, high efficiency and compati

Silver ion mediated in situ synthesis of mixed diaryl sulfides from diaryl disulfides

The AgNO3-mediated in situ scission of aromatic disulfides in the presence of electron-rich aromatic compounds results in the efficient synthesis of diaryl sulfides. Key features of this new methodology are high yields of aromatic and heteroaromatic sulfides, mild reaction conditions, simplicity, simple workup, and avoiding foul-smelling reactants like thiols. Georg Thieme Verlag Stuttgart · New York.