2-Hydroxy-6-methoxyquinoline-3-carbaldehyde

95%

Reagent Code: #197212
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CAS Number 123990-78-3

science Other reagents with same CAS 123990-78-3

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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of bioactive quinoline derivatives, particularly in pharmaceuticals with antimicrobial, antifungal, antitumor, and antioxidant properties. It serves as a building block in the development of novel heterocyclic compounds for drug discovery. Its aldehyde, hydroxyl, and methoxy functional groups allow for easy modification and binding to biomolecules such as enzymes or proteins, enabling the creation of Schiff bases and other derivatives that enhance biological activity, including inhibition of certain bacterial growth and cellular-level anticancer effects. Also employed in research focused on fluorescent probes due to its inherent photophysical properties, useful in imaging and sensor applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,460.00
250mg
10-20 days ฿7,430.00
1g
10-20 days ฿18,220.00
2-Hydroxy-6-methoxyquinoline-3-carbaldehyde
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Used as a key intermediate in the synthesis of bioactive quinoline derivatives, particularly in pharmaceuticals with antimicrobial, antifungal, antitumor, and antioxidant properties. It serves as a building block in the development of novel heterocyclic compounds for drug discovery. Its aldehyde, hydroxyl, and methoxy functional groups allow for easy modification and binding to biomolecules such as enzymes or proteins, enabling the creation of Schiff bases and other derivatives that enhance biological ac

Used as a key intermediate in the synthesis of bioactive quinoline derivatives, particularly in pharmaceuticals with antimicrobial, antifungal, antitumor, and antioxidant properties. It serves as a building block in the development of novel heterocyclic compounds for drug discovery. Its aldehyde, hydroxyl, and methoxy functional groups allow for easy modification and binding to biomolecules such as enzymes or proteins, enabling the creation of Schiff bases and other derivatives that enhance biological activity, including inhibition of certain bacterial growth and cellular-level anticancer effects. Also employed in research focused on fluorescent probes due to its inherent photophysical properties, useful in imaging and sensor applications.

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