5554-81-4

Basic information

• Product Name: Phosphorane, [[(4-methylphenyl)sulfonyl]methylene]triphenyl-
• CAS NO: 5554-81-4
• Molecular Formula: C26H23O2PS
• Molecular Weight: 430.507
• Mol File: 5554-81-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphorane, [[(4-methylphenyl)sulfonyl]methylene]triphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphorane, [[(4-methylphenyl)sulfonyl]methylene]triphenyl-(5554-81-4)
• EPA Substance Registry System: Phosphorane, [[(4-methylphenyl)sulfonyl]methylene]triphenyl-(5554-81-4)

Safety Data

• Hazardous Substances Data: 5554-81-4(Hazardous Substances Data)

Upstream product

• 455-16-3 p-toluenesulfonyl fluoride 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 37891-96-6 1-((iodom ethyl)sulfonyl)-4-methylbenzene 
• 603-35-0 triphenylphosphine 
• 62-53-3 aniline 
• 109-89-7 diethylamine 
• 109-97-7 pyrrole 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 133951-77-6 6-N-benzoyl-9-<5,6-dideoxy-2,3-O-isopropylidene-6-(p-toluenesulfonyl)-β-D-ribo-hex-5(E)-enofuranosyl>adenine 
• 133951-78-7 9-<5,6-dideoxy-2,3-O-isopropylidene-6-(p-toluenesulfonyl)-β-D-ribo-hex-5(E)-enofuranosyl>adenine 
• 139915-06-3 3-ethoxy-4,4-dimethyl-1-(p-tolylsulfonyl)-1,2-pentadiene 
• 138310-61-9 1-<5,6-dideoxy-2,3-O-isopropylidene-6-(p-toluenesulfonyl)-β-D-ribo-hex-5(E)-enofuranosyl>uracil 
• 36196-04-0 -triphenyl-phosphoran 
• 121033-91-8 (E)-4,4-dimethyl-1-tosyl-1-pentene 
• 16212-08-1 1-methyl-4-[(E)-2-phenylethenesulfonyl]benzene 
• 107922-23-6 (2,4-dichloro-trans-styryl)-p-tolyl sulfone 
• 488148-50-1 [AuCl(CH(PPh₃)(S(O)2C₆H₄Me-4))] 
• 488148-47-6 [Au(CCC₆H₅)(CH(P(C₆H₅)3(SO₂C₆H₄Me-4))] 
• 488148-71-6 [Au(CCC₆H₄OMe-4)(CH(P(C₆H₅)3(SO₂C₆H₄Me-4))] 
• 488148-74-9 [Au(CCC₆H₄CCC₆H₅-4)(CH(P(C₆H₅)3(SO₂C₆H₄Me-4))] 
• 16212-08-1 1-methyl-4-((2-phenylallyl)sulfonyl)benzene 
• 82877-02-9 <(diphenylphosphino)tosylmethylene>triphenylphosphorane 

Relevant articles and documents

Comparison of free-radical inhibiting antioxidant properties of carvedilol and its phenolic metabolites

Carvedilol is a widely prescribed drug for the treatment of heart failure and the prevention of associated ventricular arrhythmias. It has also been reported to function as a biological antioxidant via hydrogen atom transfer from its carbazole N-H moiety

Bridging the Gap between Bisylides and Methandiides: Isolation, Reactivity, and Electronic Structure of an Yldiide

Bisylides and methandiides are two unique families of carbon bases that have found a variety of applications in recent years. Metalated ylides (yldiides) are the link between these types of compounds. Yet, only little is known about their properties, reactivities, and particularly their electronic structure. Here, we report the preparation of the metalated ylide [Ph3P-C-SO2Tol]- (1) with different alkali metal counterions. The compounds have been studied by X-ray diffraction analysis and NMR spectroscopy and the first structures of a sodium and potassium yldiide are presented. The electronic structure of 1 was explored by DFT calculations confirming its relation with other divalent carbon species. Reactivity studies demonstrate the strong nucleophilicity of the yldiide and its capability to act both as a σ- and π-donor. Metalation makes a difference. The metalation of a stabilized phosphorus ylide yields the isolable yldiide [Ph3P-C-SO2Tol]-, which was isolated with different alkali metal counterions. Its electronic structure shows a clear relation to other divalent carbon species such as bisylides. Reactivity studies demonstrate the strong nucleophilicity of the yldiide and its capability to act both as a σ- and π-donor.