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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-fluoro-4-methylpyridin-3-amine

Fc1ncc(c(c1)C)N Request for Quotation
Chemical Name: 6-fluoro-4-methylpyridin-3-amine
CAS Number: 954236-33-0
Product Number: AG003N7P(AGN-PC-058CP1)
Synonyms:
MDL No:
Molecular Formula: C6H7FN2
Molecular Weight: 126.1316

Identification/Properties

Properties
MP:
57-62℃
BP:
276℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
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

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


6-Fluoro-4-methylpyridin-3-amine is a versatile compound that finds significant application in chemical synthesis. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 6-Fluoro-4-methylpyridin-3-amine can be utilized for the creation of complex molecules through the functionalization of its fluorine and amino groups. Its unique structure and reactivity enable the formation of diverse bonds and substitution reactions, making it an invaluable tool in the development of novel organic compounds.Furthermore, 6-Fluoro-4-methylpyridin-3-amine plays a vital role in the synthesis of heterocyclic compounds, which are commonly found in many biologically active molecules. By incorporating this compound into various synthetic pathways, chemists can access a wide range of chemical structures with potential pharmacological, agricultural, or material science applications.