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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)-

Acetamide, N-(5-fluoro-2-pyridinyl)-

CC(=O)Nc1ccc(cn1)F Request for Quotation
Chemical Name: Acetamide, N-(5-fluoro-2-pyridinyl)-
CAS Number: 100304-88-9
Product Number: AG0001JW(AGN-PC-05W5H4)
Synonyms:
MDL No:
Molecular Formula: C7H7FN2O
Molecular Weight: 154.1417

Identification/Properties

Properties
BP:
319.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
154.144g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
154.054g/mol
Monoisotopic Mass:
154.054g/mol
Topological Polar Surface Area:
42A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Acetamido-5-fluoropyridine is a versatile compound commonly used in chemical synthesis as a key building block. It serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound plays a crucial role in the synthesis of complex molecules due to its unique structural properties and reactivity. Specifically, 2-Acetamido-5-fluoropyridine is utilized in the preparation of heterocyclic compounds, which are essential in drug discovery and development. Its presence in the chemical synthesis process enables the modification and functionalization of organic molecules, leading to the creation of novel compounds with diverse biological activities. Additionally, the compound's fluorine substituent enhances its chemical stability and can impact the overall pharmacokinetic properties of the final products. In summary, 2-Acetamido-5-fluoropyridine is a crucial component in the synthesis of various valuable compounds with potential applications in the pharmaceutical and agricultural industries.