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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)-

N-quinolin-6-ylacetamide

CC(=O)Nc1ccc2c(c1)cccn2 Request for Quotation
Chemical Name: N-quinolin-6-ylacetamide
CAS Number: 22433-76-7
Product Number: AG00BIOK(AGN-PC-0JKLS9)
Synonyms:
MDL No:
Molecular Formula: C11H10N2O
Molecular Weight: 186.2099

Identification/Properties

Computed Properties
Molecular Weight:
186.214g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
186.079g/mol
Monoisotopic Mass:
186.079g/mol
Topological Polar Surface Area:
42A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
217
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#:
N/A
Hazard Statements:
H302-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


N-6-Quinolinylacetamide is a versatile compound frequently used in chemical synthesis due to its unique reactivity and functional group compatibility. In organic reactions, this compound serves as a valuable building block for the synthesis of various biologically active molecules, pharmaceutical intermediates, and complex organic compounds. Its quinoline moiety imparts specific properties and reactivity, making it a crucial component in the development of novel chemical entities. 
By incorporating N-6-Quinolinylacetamide into synthetic routes, chemists can introduce quinoline functionality into target molecules, leading to enhanced biological activity or specific chemical properties. Furthermore, the acetamide group offers opportunities for further derivatization, allowing for the introduction of additional functionalities to tailor the compound's properties to specific applications. Overall, the application of N-6-Quinolinylacetamide in chemical synthesis enables the efficient construction of diverse molecular scaffolds with potential therapeutic or industrial significance.