3-Pyrimidin-2-yl-benzoic acid

95%

Reagent Code: #225323
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CAS Number 579476-26-9

science Other reagents with same CAS 579476-26-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.19 g/mol
Formula C₁₁H₈N₂O₂
thermostat Physical Properties
Boiling Point 319.6°C
inventory_2 Storage & Handling
Storage Room temperature, dry

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 heterocyclic structures that interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where aromatic and nitrogen-containing systems enhance performance. Its carboxylic acid group allows for easy derivatization, enabling the creation of amides, esters, and other functional derivatives for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,170.00
inventory 1g
10-20 days ฿5,210.00

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3-Pyrimidin-2-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 heterocyclic structures that interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where aromatic and nitrogen-containing systems enhance performance. Its carboxylic acid group allows for easy derivatization, enabling the creation of ami

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 heterocyclic structures that interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where aromatic and nitrogen-containing systems enhance performance. Its carboxylic acid group allows for easy derivatization, enabling the creation of amides, esters, and other functional derivatives for structure-activity relationship studies.

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