4-(Pyridin-2-yloxy)benzoic acid

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Reagent Code: #223074
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CAS Number 51363-00-9

science Other reagents with same CAS 51363-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.2 g/mol
Formula C₁₂H₉NO₃
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MDL Number MFCD08435897
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its ability to form stable heterocyclic structures. Its carboxylic acid functionality allows for easy derivatization, enabling conjugation into larger molecules for drug discovery. Also employed in agrochemical research for designing novel herbicides and plant growth regulators. Its pyridine-oxygen-benzene scaffold enhances binding affinity in biological systems, making it valuable in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,910.00
inventory 1g
10-20 days ฿17,080.00
inventory 5g
10-20 days ฿42,700.00

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4-(Pyridin-2-yloxy)benzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its ability to form stable heterocyclic structures. Its carboxylic acid functionality allows for easy derivatization, enabling conjugation into larger molecules for drug discovery. Also employed in agrochemical research for designing novel herbicides and plant growth re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its ability to form stable heterocyclic structures. Its carboxylic acid functionality allows for easy derivatization, enabling conjugation into larger molecules for drug discovery. Also employed in agrochemical research for designing novel herbicides and plant growth regulators. Its pyridine-oxygen-benzene scaffold enhances binding affinity in biological systems, making it valuable in medicinal chemistry.

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