| Identification | More | [Name]
Bis(2-nitrophenyl) disulfide | [CAS]
1155-00-6 | [Synonyms]
2,2'-DINITRODIPHENYL DISULFIDE
2,2'-DINITRODIPHENYL DISULPHIDE
2-NITROPHENYL DISULFIDE
BIS(2-NITROPHENYL) DISULFIDE
BIS(2-NITROPHENYL) DISULPHIDE
BIS(O-NITROPHENYL) DISULFIDE
DI-2-NITROPHENYL DISULFIDE
O-DINITRODIPHENYL DISULFIDE
O-NITROPHENYLDISULFIDE
O,O'-DINITROPHENYL DISULFIDE
1-Nitro-2-[(2-nitrophenyl)disulfanyl]benzene
Bis-(2-nitrophenyl)-disulfid
Disulfide, bis(2-nitrophenyl)
Disulfide, bis(o-nitrophenyl)
Disulfide,bis(2-nitrophenyl)
o,o'-Dinitrodiphenyl disulfide
2,2'-Dinitro
Bis(2-nitropheny1)disulfide
2-NITROPHENYL DISULFIDE 95%
1,1'-Dithiobis(2-nitrobenzene) | [EINECS(EC#)]
214-581-5 | [Molecular Formula]
C12H8N2O4S2 | [MDL Number]
MFCD00007130 | [Molecular Weight]
308.33 | [MOL File]
1155-00-6.mol |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29309099 |
| Hazard Information | Back Directory | [Chemical Properties]
yellow to yellow-green crystalline powder | [Uses]
Bis(o-Nitrophenyl) Disulfide, can be used in a PVC membrane electrode as a sensor for zinc ions. It is also a building block used for the synthesis of various pharmaceutical compounds. It can be used for the preparation of a series of 4-Azaindole inhibitors of c-Met kinase. | [General Description]
PVC membrane electrode based on bis(2-nitrophenyl)disulfide carrier acts as sensor for zinc ions. Bis(2-nitrophenyl) disulphide undergoes mechanochemical grinding with bis(4-chlorophenyl)disulfide in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene catalyst via metathesis reaction to yield non-symmetrical heterodimer 4-chlorophenyl-2′-nitrophenyl disulfide. | [Purification Methods]
Purify the disulfide by recrystallisation from glacial AcOH or from *C6H6 and the yellow needles are dried in an oven at 100o until the odour of the solvent is absent. It is sparingly soluble in EtOH and Me2CO. [Bogert & Stull Org Synth Coll Vol I 220 1941, Bauer & Cymerman J Chem Soc 3434 1949, Beilstein 6 IV 1672.] |
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