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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)-

Ethanol, 2-(2-pyridinylthio)-

OCCSc1ccccn1 Request for Quotation
Chemical Name: Ethanol, 2-(2-pyridinylthio)-
CAS Number: 77555-27-2
Product Number: AG008OVJ(AGN-PC-0KKWID)
Synonyms:
MDL No:
Molecular Formula: C7H9NOS
Molecular Weight: 155.2175

Identification/Properties

Computed Properties
Molecular Weight:
155.215g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
155.04g/mol
Monoisotopic Mass:
155.04g/mol
Topological Polar Surface Area:
58.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.7
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-(Pyridin-2-ylthio)ethanol is a versatile compound that finds frequent application in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block due to its unique structure, which consists of a pyridine ring attached to a thiol group via an ethylene linker.In chemical synthesis, 2-(Pyridin-2-ylthio)ethanol is commonly used as a reagent for the introduction of the pyridylthio functionality into various organic molecules. This functional group can serve as a key handle for further elaboration through a variety of synthetic transformations, including cross-coupling reactions, nucleophilic substitution, and metal-catalyzed transformations.Furthermore, the thiol group in 2-(Pyridin-2-ylthio)ethanol can participate in thiol-ene reactions, enabling the selective modification of double bonds in organic substrates. This reactivity can be harnessed for the construction of complex molecular architectures and the synthesis of biologically active compounds, making 2-(Pyridin-2-ylthio)ethanol a valuable tool in the arsenal of synthetic chemists.