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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)-

(1S)-1-(5-fluoropyridin-2-yl)ethanamine

Fc1ccc(nc1)C(N)C Request for Quotation
Chemical Name: (1S)-1-(5-fluoropyridin-2-yl)ethanamine
CAS Number: 915720-57-9
Product Number: AG00H2Q5(AGN-PC-00SZE3)
Synonyms:
MDL No:
Molecular Formula: C7H9FN2
Molecular Weight: 140.1582

Identification/Properties

Computed Properties
Molecular Weight:
140.161g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
140.075g/mol
Monoisotopic Mass:
140.075g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(5-Fluoropyridin-2-yl)ethanamine, commonly referred to as $name$, is a versatile building block in chemical synthesis. Its unique structure makes it a valuable reagent in various organic transformations. This compound can be utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. Its presence of the functional amine group allows for selective derivatization, enabling the introduction of different substituents to tailor the properties of the final product. In addition, the fluoropyridine moiety confers specific reactivity and can participate in diverse coupling reactions, facilitating the synthesis of complex molecular architectures. The application of 1-(5-Fluoropyridin-2-yl)ethanamine in chemical synthesis extends beyond its role as a simple building block, showcasing its significance in the creation of novel and valuable compounds with potential applications across various industries.