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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)-

3-Quinolinecarboxylic acid, 4-hydroxy-6-methoxy-

COc1ccc2c(c1)c(O)c(cn2)C(=O)O Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 4-hydroxy-6-methoxy-
CAS Number: 28027-16-9
Product Number: AG003LIK(AGN-PC-0O8JPO)
Synonyms:
MDL No:
Molecular Formula: C11H9NO4
Molecular Weight: 219.1935

Identification/Properties

Properties
MP:
278-279℃ (decomp)
BP:
411°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
219.196g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
219.053g/mol
Monoisotopic Mass:
219.053g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
350
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


4-Hydroxy-6-methoxyquinoline-3-carboxylic acid, also known as $name$, is a versatile compound widely employed in chemical synthesis due to its unique properties. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, $name$ acts as a key building block in the formation of complex organic molecules through its ability to participate in diverse chemical reactions.One of the primary applications of 4-Hydroxy-6-methoxyquinoline-3-carboxylic acid in chemical synthesis is as a precursor in the synthesis of heterocyclic compounds. By incorporating $name$ into the chemical reaction pathway, chemists can introduce structural diversity and functional groups into the final products, enhancing their biological activity and properties. Additionally, this compound serves as a valuable intermediate in the synthesis of quinoline derivatives, which are known for their wide range of biological and pharmacological activities.Furthermore, 4-Hydroxy-6-methoxyquinoline-3-carboxylic acid is utilized in the development of novel anticancer agents, antimicrobial compounds, and antioxidants. Its unique chemical structure enables the modification of key functional groups, leading to the creation of molecules with specific biological targets and enhanced efficacy. The versatility of $name$ in chemical synthesis makes it an indispensable tool for the creation of diverse molecular architectures with potential applications in the pharmaceutical and agrochemical industries.