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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)-

5-chloroquinoline-3-carboxylic acid

OC(=O)c1cnc2c(c1)c(Cl)ccc2 Request for Quotation
Chemical Name: 5-chloroquinoline-3-carboxylic acid
CAS Number: 1416439-55-8
Product Number: AG001GSA(AGN-PC-0JK1IM)
Synonyms:
MDL No:
Molecular Formula: C10H6ClNO2
Molecular Weight: 207.6131

Identification/Properties

Computed Properties
Molecular Weight:
207.613g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
207.009g/mol
Monoisotopic Mass:
207.009g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
234
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


5-Chloroquinoline-3-carboxylic acid is a versatile compound commonly utilized in chemical synthesis as a key building block for the production of various pharmaceuticals, agrochemicals, and functional materials. This chemical intermediate plays a crucial role in the creation of diverse molecular structures due to its unique reactivity and ability to undergo various synthetic transformations. By serving as a starting material in organic reactions, 5-Chloroquinoline-3-carboxylic acid enables the introduction of key functional groups and structural motifs, facilitating the development of novel compounds with specific desired properties. Moreover, its incorporation in multi-step synthesis sequences allows for the efficient construction of complex molecules with desired pharmacological, biological, or materials-related activities. Its versatile nature and strategic placement within synthetic pathways make 5-Chloroquinoline-3-carboxylic acid an indispensable component in the synthesis of a wide range of valuable chemical products.