5-fluoro-4-methylpyridin-2-amine|301222-66-2,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

5-fluoro-4-methylpyridin-2-amine

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Chemical Name:	5-fluoro-4-methylpyridin-2-amine
CAS Number:	301222-66-2
Product Number:	AG007JI0(AGN-PC-03JUVM)
Synonyms:
MDL No:
Molecular Formula:	C6H7FN2
Molecular Weight:	126.1316

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

126.134g/mol

XLogP3:

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

126.059g/mol

Monoisotopic Mass:

126.059g/mol

Topological Polar Surface Area:

38.9A^2

Heavy Atom Count:

Formal Charge:

Complexity:

97.1

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure

5-Fluoro-4-methylpyridin-2-amine, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block in the creation of various compounds. This compound is utilized in the formation of complex molecules through its involvement in reactions such as nucleophilic substitution, Suzuki coupling, and reductive amination. Its unique structure enables it to serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, $name$ plays a significant role in the development of novel derivatives with enhanced properties and functionalities, making it a valuable tool for researchers and chemists in the quest for new chemical entities.