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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-Quinolinecarboxamide

NC(=O)c1ccc2c(c1)cccn2 Request for Quotation
Chemical Name: 6-Quinolinecarboxamide
CAS Number: 5382-43-4
Product Number: AG00DKUV(AGN-PC-0NF35I)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O
Molecular Weight: 172.1833

Identification/Properties

Computed Properties
Molecular Weight:
172.187g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
172.064g/mol
Monoisotopic Mass:
172.064g/mol
Topological Polar Surface Area:
56A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
205
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


6-Quinolinecarboxamide, also known as "$name$", is a versatile compound widely utilized in chemical synthesis procedures. In organic chemistry, 6-Quinolinecarboxamide serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable building block for the synthesis of diverse compounds.One of the primary applications of 6-Quinolinecarboxamide in chemical synthesis is its role as a precursor in the preparation of heterocyclic compounds. By undergoing various functional group transformations, 6-Quinolinecarboxamide can be modified to introduce specific functionalities or structural motifs into the target molecules. This flexibility allows chemists to access a wide range of compounds with tailored properties and applications.Furthermore, 6-Quinolinecarboxamide can participate in key synthetic reactions such as nucleophilic substitution, oxidative coupling, and palladium-catalyzed cross-coupling reactions. These transformations enable the construction of complex molecular architectures with high efficiency and selectivity. Additionally, the presence of the quinoline ring in 6-Quinolinecarboxamide provides opportunities for further diversification through functional group modification or ring-closure reactions.Overall, the use of 6-Quinolinecarboxamide in chemical synthesis offers a strategic approach to accessing structurally diverse and biologically relevant compounds. Its versatile nature and synthetic utility make it a valuable tool for organic chemists seeking to design and develop novel molecules for various applications in the pharmaceutical, agricultural, and materials science industries.