1. Home
  2. 3-Quinolinecarboxylic acid, 4-chloro-6-fluoro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

3-Quinolinecarboxylic acid, 4-chloro-6-fluoro-

Fc1ccc2c(c1)c(Cl)c(cn2)C(=O)O Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 4-chloro-6-fluoro-
CAS Number: 179024-67-0
Product Number: AG0026PD(AGN-PC-0KUJPT)
Synonyms:
MDL No:
Molecular Formula: C10H5ClFNO2
Molecular Weight: 225.6036

Identification/Properties

Computed Properties
Molecular Weight:
225.603g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
224.999g/mol
Monoisotopic Mass:
224.999g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
264
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

Request for Quotation

Customer Feedback

Chemical Structure


4-Chloro-6-fluoroquinoline-3-carboxylic acid, also known as $name$, is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structural properties. In organic synthesis, $name$ can undergo various chemical reactions such as substitution, condensation, and cyclization to form complex molecular structures. Its fluorine and chlorine substituents make it a valuable intermediate in the synthesis of heterocyclic compounds and biologically active molecules. Additionally, the carboxylic acid group provides a convenient handle for further functionalization, enabling the modification of its chemical properties for specific applications. With its diverse reactivity and compatibility with a wide range of synthetic methodologies, 4-Chloro-6-fluoroquinoline-3-carboxylic acid is an essential component in the development of novel chemical compounds with potential therapeutic, agricultural, and industrial applications.