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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)-

2-Naphthalenol, 6,6'-dithiobis-

Oc1ccc2c(c1)ccc(c2)SSc1ccc2c(c1)ccc(c2)O Request for Quotation
Chemical Name: 2-Naphthalenol, 6,6'-dithiobis-
CAS Number: 6088-51-3
Product Number: AG003N8G(AGN-PC-0JKGHN)
Synonyms:
MDL No:
Molecular Formula: C20H14O2S2
Molecular Weight: 350.4540

Identification/Properties

Properties
MP:
226 °C
Form:
Solid
Computed Properties
Molecular Weight:
350.45g/mol
XLogP3:
5.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
350.044g/mol
Monoisotopic Mass:
350.044g/mol
Topological Polar Surface Area:
91.1A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
380
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,6'-Disulfanediylbis(naphthalen-2-ol) is a versatile compound commonly used in chemical synthesis as a potent catalyst. This compound plays a crucial role in various reactions due to its unique structural properties, which facilitate the formation of complex organic molecules. In chemical synthesis, 6,6'-Disulfanediylbis(naphthalen-2-ol) acts as a key reagent for promoting important transformations, such as aromatic substitutions, cyclization reactions, and oxidative coupling processes. Its ability to facilitate selective C-S bond formations and enhance stereochemistry makes it an indispensable tool for advanced synthetic processes in organic chemistry. Additionally, this compound exhibits excellent stability and reactivity under a wide range of reaction conditions, making it an ideal choice for designing and optimizing synthetic routes for the production of pharmaceuticals, agrochemicals, and materials with high purity and efficiency.