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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)-

4-methylsulfanylpyridine-2-carbonitrile

CSc1ccnc(c1)C#N Request for Quotation
Chemical Name: 4-methylsulfanylpyridine-2-carbonitrile
CAS Number: 501379-24-4
Product Number: AG006VUL(AGN-PC-02RRX0)
Synonyms:
MDL No:
Molecular Formula: C7H6N2S
Molecular Weight: 150.2009

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
150.199g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
150.025g/mol
Monoisotopic Mass:
150.025g/mol
Topological Polar Surface Area:
62A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
149
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


4-(Methylthio)picolinonitrile is a versatile compound widely used in chemical synthesis for its unique properties and applications. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. Its inherent chemical reactivity makes it a key intermediate in the synthesis of complex organic compounds.One common application of 4-(Methylthio)picolinonitrile is in the preparation of heterocyclic compounds, particularly pyridine derivatives. By incorporating this compound into chemical reactions, chemists can effectively introduce the methylthio group into the molecular structure, leading to the formation of novel compounds with diverse properties and functionalities.Furthermore, 4-(Methylthio)picolinonitrile can also be utilized in the synthesis of bioactive molecules and pharmaceutical intermediates. Its unique structure allows for the modification of functional groups, enabling the production of tailored compounds with specific biological activities.In summary, the application of 4-(Methylthio)picolinonitrile in chemical synthesis plays a crucial role in the development of new materials, pharmaceuticals, and specialty chemicals. Its versatility and reactivity make it a valuable tool for organic chemists seeking to create innovative compounds with tailored properties.