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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)-

2,6-Naphthalenedithiol

Sc1ccc2c(c1)ccc(c2)S Request for Quotation
Chemical Name: 2,6-Naphthalenedithiol
CAS Number: 96892-95-4
Product Number: AG006OI7(AGN-PC-00M7CH)
Synonyms:
MDL No:
Molecular Formula: C10H8S2
Molecular Weight: 192.3005

Identification/Properties

Computed Properties
Molecular Weight:
192.294g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
192.007g/mol
Monoisotopic Mass:
192.007g/mol
Topological Polar Surface Area:
2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
140
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


2,6-Naphthalenedithiol, also known as NDT, is a versatile compound widely used in various chemical synthesis applications. As a key building block in organic chemistry, this compound is valued for its ability to form strong covalent bonds with a variety of metal ions, making it a crucial reagent in the preparation of metal coordination complexes.In chemical synthesis, 2,6-Naphthalenedithiol plays a crucial role in the creation of metal-sulfur clusters, which are essential in the development of catalysts, sensors, and materials with unique electronic and optical properties. Its strong chelating capabilities enable the selective binding of metal ions, facilitating the formation of complex structures with tailored properties.Additionally, 2,6-Naphthalenedithiol is commonly employed in the modification of surfaces and nanoparticles, enabling the functionalization of materials for various applications such as sensing, catalysis, and electronic devices. Its ability to anchor metal ions onto surfaces makes it a valuable tool in surface chemistry and nanotechnology.Overall, the versatile nature of 2,6-Naphthalenedithiol makes it a fundamental component in chemical synthesis, enabling the development of novel materials and compounds with tailored properties and applications.