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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)-

6-(Ttrifluoromethylthio)pyridin-3-amine

Nc1ccc(nc1)SC(F)(F)F Request for Quotation
Chemical Name: 6-(Ttrifluoromethylthio)pyridin-3-amine
CAS Number: 1153767-25-9
Product Number: AG0095G9(AGN-PC-0WAKFN)
Synonyms:
MDL No:
Molecular Formula: C6H5F3N2S
Molecular Weight: 194.1775

Identification/Properties

Computed Properties
Molecular Weight:
194.175g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
194.013g/mol
Monoisotopic Mass:
194.013g/mol
Topological Polar Surface Area:
64.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
150
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


6-((Trifluoromethyl)thio)pyridin-3-amine is a versatile compound frequently utilized in various chemical synthesis applications. Its unique structure containing a trifluoromethylthio group attached to a pyridine ring offers specific reactivity and functional properties that make it valuable in organic chemistry endeavors. This compound serves as a crucial building block in the creation of complex organic molecules, particularly in the development of pharmaceuticals, agrochemicals, and material science. With its ability to participate in diverse reactions and form key intermediates, 6-((Trifluoromethyl)thio)pyridin-3-amine plays a vital role in the strategic design and synthesis of novel compounds with enhanced bioactivity or material properties. Its utility extends to the creation of specialized ligands, catalysts, and bioconjugates, showcasing its significance in advancing the frontier of chemical synthesis methodologies.