CAS 373384-17-9
:2-(4-Boronophenyl)-4-quinolinecarboxylic acid
Description:
2-(4-Boronophenyl)-4-quinolinecarboxylic acid is an organic compound characterized by the presence of both a boron-containing moiety and a quinoline structure. This compound features a quinoline ring, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring, and a carboxylic acid functional group that contributes to its acidity and potential reactivity. The boron atom is typically involved in coordination chemistry, making this compound of interest in various applications, including materials science and medicinal chemistry. The presence of the boron phenyl group can enhance the compound's electronic properties, potentially making it useful in organic electronics or as a ligand in coordination complexes. Additionally, the compound may exhibit interesting photophysical properties due to its conjugated system, which can be exploited in fluorescence or phosphorescence applications. Overall, 2-(4-Boronophenyl)-4-quinolinecarboxylic acid is a versatile compound with potential applications in various fields of chemistry and materials science.
Formula:C16H12BNO4
InChI:InChI=1S/C16H12BNO4/c19-16(20)13-9-15(18-14-4-2-1-3-12(13)14)10-5-7-11(8-6-10)17(21)22/h1-9,21-22H,(H,19,20)
InChI key:InChIKey=QSHXLXJUIBYXKH-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C2=C(N=C(C1)C3=CC=C(B(O)O)C=C3)C=CC=C2
Synonyms:- 2-(4-Dihydroxyborane)phenyl-4-carboxyquinoline
- 4-Quinolinecarboxylic acid, 2-(4-boronophenyl)-
- 2-(4-Boronophenyl)-4-quinolinecarboxylic acid
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Found 3 products.
2-(4-Dihydroxyborane)phenyl-4-carboxyquinoline
CAS:Formula:C16H12BNO4Purity:97%Color and Shape:SolidMolecular weight:293.08182-(4-Boronophenyl)quinoline-4-carboxylic acid
CAS:2-(4-Boronophenyl)quinoline-4-carboxylic acidPurity:97%Molecular weight:293.08g/mol2-(4-DIHYDROXYBORANE)PHENYL-4-CARBOXYQUINOLINE PINACOL ESTER
CAS:Formula:C22H22BNO4Purity:95.0%Molecular weight:375.23


