3-(pyridin-4-yl)benzoic acid

95%

Reagent Code: #224941
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CAS Number 4385-78-8

science Other reagents with same CAS 4385-78-8

blur_circular Chemical Specifications

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Weight 199.21 g/mol
Formula C₁₂H₉NO₂
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MDL Number MFCD05864808
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable aromatic and heterocyclic frameworks. Commonly employed in cross-coupling reactions to construct biaryl systems found in bioactive molecules. Also utilized in the preparation of ligands for metal-catalyzed reactions, enhancing catalytic efficiency in organic synthesis. Its carboxylic acid functionality allows for easy derivatization into amides, esters, and other functional groups for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿3,280.00
inventory 5g
10-20 days ฿9,280.00

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3-(pyridin-4-yl)benzoic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable aromatic and heterocyclic frameworks. Commonly employed in cross-coupling reactions to construct biaryl systems found in bioactive molecules. Also utilized in the preparation of ligands for metal-catalyzed reactions, enhancing catalytic efficiency in organic synthesis. Its carboxylic acid funct
Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable aromatic and heterocyclic frameworks. Commonly employed in cross-coupling reactions to construct biaryl systems found in bioactive molecules. Also utilized in the preparation of ligands for metal-catalyzed reactions, enhancing catalytic efficiency in organic synthesis. Its carboxylic acid functionality allows for easy derivatization into amides, esters, and other functional groups for structure-activity relationship studies.
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