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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)-

3-Pyridinamine, 6-fluoro-5-methyl-

Nc1cnc(c(c1)C)F Request for Quotation
Chemical Name: 3-Pyridinamine, 6-fluoro-5-methyl-
CAS Number: 186593-48-6
Product Number: AG00AOFI(AGN-PC-03I7Z2)
Synonyms:
MDL No:
Molecular Formula: C6H7FN2
Molecular Weight: 126.1316

Identification/Properties

Computed Properties
Molecular Weight:
126.134g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
126.059g/mol
Monoisotopic Mass:
126.059g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
97.1
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-Fluoro-5-methylpyridin-3-amine, also known by its chemical formula C6H7FN2, is a versatile compound widely used in chemical synthesis applications. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.One of the primary applications of 6-Fluoro-5-methylpyridin-3-amine is its role as a precursor in the synthesis of pharmaceutical compounds. By incorporating this compound into organic reactions, chemists can introduce the fluorine and amino functional groups into the target molecules, enhancing their biological activity and pharmacokinetic properties. This makes 6-Fluoro-5-methylpyridin-3-amine an invaluable intermediate in the development of new drugs for the treatment of various diseases.Furthermore, this compound can be utilized in the synthesis of agrochemicals, such as pesticides and herbicides. The fluorine moiety in 6-Fluoro-5-methylpyridin-3-amine can impart desirable properties to these agricultural chemicals, increasing their effectiveness and stability. By incorporating this building block into the molecular structure of agrochemicals, researchers can improve their performance in protecting crops and enhancing agricultural productivity.Moreover, 6-Fluoro-5-methylpyridin-3-amine finds applications in material science, where it can be used to create functional materials with tailored properties. By utilizing this compound as a starting material in polymerization or cross-coupling reactions, scientists can engineer new materials with specific characteristics, such as enhanced conductivity, optical properties, or mechanical strength. This versatility makes 6-Fluoro-5-methylpyridin-3-amine a valuable tool in the design and synthesis of advanced materials for various industrial applications.