CAS 882-33-7
:Disulfure de diphényle
- (Phenyldisulfanyl)benzene
- 1,1'-Diphenyl disulfide
- 1,1'-Disulfanediyldibenzene
- 1,1′-Dithiodibenzene
- 1,2-Diphenyldisulfane
- Biphenyl disulfide
- Diphenyl disulfide
- Diphenyl disulphide
- Diphenyldisulfid
- Disulfide, diphenyl
- Disulfure de diphenyle
- Disulfuro De Difenilo
- Nsc 2689
- Phenyl disulphide
- Voir plus de synonymes
Diphenyl Disulfide
CAS :Formule :C12H10S2Degré de pureté :>99.0%(GC)Couleur et forme :White to Light yellow powder to crystalMasse moléculaire :218.33Diphenyl disulfide, 98%
CAS :Diphenyl disulfide is one of the most popular organic disulfides used in organic synthesis. It is used as a reagent for the -phenylsulfenylation of carbonyl compounds. It participates in hydrothiolation of alkynes via amine-mediated single electron transfer mechanism. It is the hydrolysis product ofFormule :C12H10S2Degré de pureté :98%Couleur et forme :White to cream, Crystals or powder or crystalline powder or fused solidMasse moléculaire :218.33Phenyl disulfide
CAS :Formule :C12H10S2Degré de pureté :(GC) ≥ 99.0%Couleur et forme :Off-white to light yellow crystalline powder or crystalsMasse moléculaire :218.34Diphenyl disulfide
CAS :Diphenyl disulfide fights breast cancer by inducing cell death and stopping growth.Formule :C12H10S2Degré de pureté :99.95%Couleur et forme :White To Light Yellow CrystalMasse moléculaire :218.34Diphenyl Disulfide
CAS :Produit contrôléApplications Diphenyl Disulfide is used in the synthesis of bis-vinyl selenides displaying antinociceptive activity. Also used in the preparation of potent poxvirus inhibitors, particularly smalllpox.
References Sartori, G. et al.: Org. Biomol. Chem., 11, 1199 (2013); Nuth, M. et al.: J. Med. CHem., 56, (2013);Formule :C12H10S2Couleur et forme :Off-WhiteMasse moléculaire :218.34Diphenyl disulfide
CAS :Formule :C12H10S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :218.33Diphenyl disulfide
CAS :Diphenyl disulfide is a chemical compound that is synthesized by the reaction of diphenyl with hydrochloric acid, followed by the addition of aryl halides. The reaction mechanism for this process involves hydrogen bonding interactions and hydroxyl group reactions. Disulfides are also formed in the synthesis of other chemicals, such as thiophene and benzene. Synthesis methods for this compound include the palladium-catalyzed coupling of two aryl halides and an intramolecular hydrogen transfer reaction. Diphenyl disulfide has been shown to have x-ray crystal structures with a molecular weight of 188.2 g/mol and a molecular formula of C14H10S2.
Formule :C12H10S2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :218.34 g/mol










