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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)-

Pyridine, 2-(methylsulfinyl)-

CS(=O)c1ccccn1 Request for Quotation
Chemical Name: Pyridine, 2-(methylsulfinyl)-
CAS Number: 21948-75-4
Product Number: AG006YG8(AGN-PC-0JNKSL)
Synonyms:
MDL No:
Molecular Formula: C6H7NOS
Molecular Weight: 141.1909

Identification/Properties

Computed Properties
Molecular Weight:
141.188g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
141.025g/mol
Monoisotopic Mass:
141.025g/mol
Topological Polar Surface Area:
49.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
116
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-(Methylsulfinyl)pyridine is a versatile organic compound commonly used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. This compound is known for its unique structure, which incorporates a pyridine ring with a methylsulfinyl group attached at the 2-position.In chemical synthesis, 2-(Methylsulfinyl)pyridine serves as a valuable reagent for the construction of complex molecular structures due to its ability to participate in a wide range of reactions. Its sulfone functionality provides a site for introducing diverse chemical modifications, enabling the synthesis of novel compounds with desired properties. Additionally, the presence of the pyridine ring enhances the compound's reactivity and allows for the development of stereochemically complex molecules.Researchers and chemists often utilize 2-(Methylsulfinyl)pyridine in the synthesis of bioactive compounds, such as pharmaceutical intermediates and natural product derivatives. By strategically incorporating this compound into synthetic routes, chemists can access a diverse array of molecular scaffolds with potential applications in drug discovery, medical research, and agricultural chemistry.Overall, the application of 2-(Methylsulfinyl)pyridine in chemical synthesis underscores its significance as a valuable building block for the creation of structurally diverse and biologically relevant compounds. Whether in the laboratory or industrial setting, this compound plays a crucial role in advancing the field of organic chemistry and expanding the possibilities for creating innovative molecules with therapeutic and commercial potential.