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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-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile

COc1cc2c(cc1OCc1ccccc1)ncc(c2O)C#N Request for Quotation
Chemical Name: 7-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile
CAS Number: 214476-89-8
Product Number: AG00BF19(AGN-PC-0WAI38)
Synonyms:
MDL No:
Molecular Formula: C18H14N2O3
Molecular Weight: 306.3154

Identification/Properties

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-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile is a versatile compound commonly used in chemical synthesis as a building block for the production of various pharmaceuticals and fine chemicals. Due to its unique molecular structure, this compound serves as a valuable intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical industry.One important application of 7-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile is as a key intermediate in the synthesis of quinoline-based drugs. Quinoline derivatives have shown promising pharmacological activities, including antimalarial, antibacterial, and anticancer properties. By utilizing 7-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile as a starting material, chemists can introduce various functional groups and modifications to tailor the molecular structure of the final pharmaceutical compound, thereby enhancing its desired biological activity and pharmacokinetic properties.Furthermore, the presence of the benzyloxy, hydroxy, methoxy, and cyano groups in 7-(Benzyloxy)-4-hydroxy-6-methoxyquinoline-3-carbonitrile provides multiple synthetic handles for further derivatization, allowing for the preparation of diverse analogs and derivatives with potential therapeutic applications. This compound's role in chemical synthesis highlights its significance in drug discovery and development efforts, showcasing its value as a versatile and crucial building block in organic chemistry.