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Diphenyl disulfide

CAS No.:
882-33-7
Catalog Number:
AG0035GY
Molecular Formula:
C12H10S2
Molecular Weight:
218.3378
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$25
- +
25g
95%
In Stock USA
United States
$47
- +
100g
95%
In Stock USA
United States
$75
- +
500g
95%
In Stock USA
United States
$172
- +
Product Description
Catalog Number:
AG0035GY
Chemical Name:
Diphenyl disulfide
CAS Number:
882-33-7
Molecular Formula:
C12H10S2
Molecular Weight:
218.3378
MDL Number:
MFCD00003065
IUPAC Name:
(phenyldisulfanyl)benzene
InChI:
InChI=1S/C12H10S2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
InChI Key:
GUUVPOWQJOLRAS-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)SSc1ccccc1
EC Number:
212-926-4
UNII:
7P54H519IJ
NSC Number:
2689
FEMA Number:
3225
Properties
Complexity:
128  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
218.022g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
218.332g/mol
Monoisotopic Mass:
218.022g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
50.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.4  
Literature
Title Journal
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Capillary electrophoresis with laser induced-fluorescence detection of profens derivatized with the water-soluble fluorogenic reagent 4-N-(4-N'-aminoethyl)piperazino-7-nitro-2,1,3-benzoxadiazole. Journal of chromatography. A 20030905
Investigating the origin of the slow-binding inhibition of HCV NS3 serine protease by a novel substrate based inhibitor. Biochemistry 20030729
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Diazenecarboxamide UP-91, a potential anticancer agent, acts by reducing cellular glutathione content. Pharmacology & toxicology 20021101
Lead(II)-selective electrode based on phenyl disulfide. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20020901
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Diphenyl disulfide and sodium in NMP as an efficient protocol for in situ generation of thiophenolate anion: selective deprotection of aryl alkyl ethers and alkyl/aryl esters under nonhydrolytic conditions. The Journal of organic chemistry 20020322
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Properties