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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)-

5-fluoro-2-methoxypyridin-3-amine

COc1ncc(cc1N)F Request for Quotation
Chemical Name: 5-fluoro-2-methoxypyridin-3-amine
CAS Number: 1211541-93-3
Product Number: AG009WJL(AGN-PC-0J0YB5)
Synonyms:
MDL No:
Molecular Formula: C6H7FN2O
Molecular Weight: 142.1310

Identification/Properties

Computed Properties
Molecular Weight:
142.133g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
142.054g/mol
Monoisotopic Mass:
142.054g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-2-methoxypyridin-3-amine is a versatile compound widely used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique molecular structure and reactivity, this compound plays a crucial role in the creation of complex organic molecules through derivatization and functional group transformations. In particular, 5-Fluoro-2-methoxypyridin-3-amine is valued for its ability to serve as a precursor in the synthesis of biologically active compounds, such as potential drug candidates or intermediates for advanced materials. Its incorporation into target molecules can lead to enhanced pharmacological properties, improved selectivity, and fine-tuning of chemical characteristics. Chemists leverage the versatility of 5-Fluoro-2-methoxypyridin-3-amine to introduce specific functionalities, modify molecular scaffolds, and explore novel synthetic pathways, ultimately enabling the development of innovative compounds with diverse applications in the fields of medicine, agriculture, and materials science.