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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)-

7-methylquinoline-3-carboxylic acid

Cc1ccc2c(c1)ncc(c2)C(=O)O Request for Quotation
Chemical Name: 7-methylquinoline-3-carboxylic acid
CAS Number: 948291-17-6
Product Number: AG006S0W(AGN-PC-01A9QG)
Synonyms:
MDL No:
Molecular Formula: C11H9NO2
Molecular Weight: 187.1947

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
187.198g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
187.063g/mol
Monoisotopic Mass:
187.063g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
229
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


7-Methylquinoline-3-carboxylic acid, also known as 7-MQA, is a versatile intermediate commonly used in chemical synthesis. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and functional materials due to its unique chemical properties.In chemical synthesis, 7-Methylquinoline-3-carboxylic acid serves as a key building block for the construction of complex organic molecules. Its functional groups and structural features make it a valuable starting material for the synthesis of a wide range of bioactive compounds, including antiviral agents, antibacterial drugs, and anti-inflammatory medications.One of the primary applications of 7-MQA in chemical synthesis is its use as a precursor for the synthesis of quinoline derivatives. By modifying the parent molecule, chemists can fine-tune the properties and biological activities of the resulting compounds. This flexibility allows for the development of new drugs with improved efficacy, selectivity, and safety profiles.Furthermore, 7-Methylquinoline-3-carboxylic acid can be utilized in the synthesis of metal complexes for catalytic reactions and materials science applications. Its ability to coordinate with metal ions enables the formation of stable complexes that exhibit unique reactivity and properties. These metal-quinoline complexes have been employed in various organic transformations and material synthesis processes, showcasing the diverse utility of 7-MQA in chemical research and development.Overall, the versatility and reactivity of 7-Methylquinoline-3-carboxylic acid make it a valuable tool in chemical synthesis, enabling the creation of novel compounds with potential applications in pharmaceuticals, agrochemicals, and advanced materials.