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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzamide, N,N'-(dithiodiphenylene)bis-

O=C(c1ccccc1)Nc1ccccc1SSc1ccccc1NC(=O)c1ccccc1 Request for Quotation
Chemical Name: Benzamide, N,N'-(dithiodiphenylene)bis-
CAS Number: 135-57-9
Product Number: AG003FCA(AGN-PC-0JL7PJ)
Synonyms:
MDL No:
Molecular Formula: C26H20N2O2S2
Molecular Weight: 456.5792

Identification/Properties

Properties
MP:
143-146°C
BP:
511.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.6360 (estimate)
Computed Properties
Molecular Weight:
456.578g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
456.097g/mol
Monoisotopic Mass:
456.097g/mol
Topological Polar Surface Area:
109A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
553
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bis(2-benzamidophenyl) Disulfide is a versatile compound widely used in chemical synthesis as a powerful reagent for the formation of disulfide bonds. This compound plays a crucial role in organic chemistry by facilitating thiol-disulfide exchange reactions, which are vital in the synthesis of various sulfur-containing compounds. Additionally, Bis(2-benzamidophenyl) Disulfide can act as a thiol-blocking agent, preventing undesired thiol oxidation during chemical reactions. Its unique structure and reactivity make it a valuable tool in the preparation of pharmaceutical intermediates, polymers, and functional materials.