3-(Benzyloxy)-5-bromopicolinic acid

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Reagent Code: #152360
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CAS Number 1393534-89-8

science Other reagents with same CAS 1393534-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.13 g/mol
Formula C₁₃H₁₀BrNO₃
badge Registry Numbers
MDL Number MFCD29058839
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromo and carboxylic acid functional groups allow for further chemical modifications, enabling coupling reactions and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to serve as a building block in heterocyclic systems. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators in research settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,180.00
inventory 250mg
10-20 days ฿9,610.00
inventory 1g
10-20 days ฿33,630.00

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3-(Benzyloxy)-5-bromopicolinic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromo and carboxylic acid functional groups allow for further chemical modifications, enabling coupling reactions and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to serve as a building block in heterocyclic systems. Also utilized in the preparation o

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromo and carboxylic acid functional groups allow for further chemical modifications, enabling coupling reactions and ring transformations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to serve as a building block in heterocyclic systems. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators in research settings.

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