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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)-

4-Quinolinecarboxylic acid, 2-(3-chlorophenyl)-

Clc1cccc(c1)c1nc2ccccc2c(c1)C(=O)O Request for Quotation
Chemical Name: 4-Quinolinecarboxylic acid, 2-(3-chlorophenyl)-
CAS Number: 20389-10-0
Product Number: AG002965(AGN-PC-0JP2AV)
Synonyms:
MDL No:
Molecular Formula: C16H10ClNO2
Molecular Weight: 283.7091

Identification/Properties

Computed Properties
Molecular Weight:
283.711g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
283.04g/mol
Monoisotopic Mass:
283.04g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
362
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


The 2-(3-Chlorophenyl)quinoline-4-carboxylic acid is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its presence enables the synthesis of novel organic molecules with diverse applications in the fields of medicine, agriculture, and materials science. In chemical synthesis, this compound plays a key role as a precursor in the formation of complex structures, contributing to the development of new and innovative products with enhanced properties. Its incorporation into synthetic pathways allows for the efficient production of advanced chemical compounds with specific functions and characteristics, making it a valuable tool for researchers and chemists in their quest for novel chemical entities and materials.