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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-formyl-2-pyridinyl)-

O=Cc1ccc(nc1)NC(=O)C Request for Quotation
Chemical Name: Acetamide, N-(5-formyl-2-pyridinyl)-
CAS Number: 149141-11-7
Product Number: AG001LF6(AGN-PC-03KKOM)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O2
Molecular Weight: 164.1613

Identification/Properties

Computed Properties
Molecular Weight:
164.164g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
164.059g/mol
Monoisotopic Mass:
164.059g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
182
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(5-Formylpyridin-2-yl)acetamide, commonly known as $name$, is a versatile compound widely used in chemical synthesis. With its unique structure and properties, $name$ plays a crucial role in various synthetic processes, particularly in the production of pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, $name$ serves as a key intermediate in the preparation of diverse organic compounds. Its functional groups enable it to participate in a range of reactions, such as condensation, alkylation, and oxidation, making it a valuable building block for designing complex molecular structures.Moreover, the presence of the formyl and pyridine moieties in $name$ imparts specific reactivity and selectivity, allowing chemists to modify its structure to tailor the properties of the final products. This versatility makes $name$ a popular choice in the synthesis of novel compounds with desired functions and properties.Overall, the application of N-(5-Formylpyridin-2-yl)acetamide in chemical synthesis showcases its significance in modern organic chemistry, offering a wide range of possibilities for creating new materials and molecules with potential applications across various industries.