3-benzyloxy-5-hydroxy-4-iodo-benzoic acid methyl ester

Reagent Code: #44632
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CAS Number 338455-12-2

science Other reagents with same CAS 338455-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.17 g/mol
Formula C₁₅H₁₃IO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a benzyloxy group, hydroxyl group, iodo substituent, and ester functionality, makes it a versatile building block in medicinal chemistry and pharmaceutical research. It is often employed in the development of drug candidates, particularly in the synthesis of compounds with potential biological activity. The iodo group allows for further functionalization through cross-coupling reactions, while the ester can be hydrolyzed to yield carboxylic acids for additional modifications. Its applications extend to the study of biochemical pathways and the design of enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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3-benzyloxy-5-hydroxy-4-iodo-benzoic acid methyl ester
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a benzyloxy group, hydroxyl group, iodo substituent, and ester functionality, makes it a versatile building block in medicinal chemistry and pharmaceutical research. It is often employed in the development of drug candidates, particularly in the synthesis of compounds with potential biological activity. The iodo group allows for further functionalization thro

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a benzyloxy group, hydroxyl group, iodo substituent, and ester functionality, makes it a versatile building block in medicinal chemistry and pharmaceutical research. It is often employed in the development of drug candidates, particularly in the synthesis of compounds with potential biological activity. The iodo group allows for further functionalization through cross-coupling reactions, while the ester can be hydrolyzed to yield carboxylic acids for additional modifications. Its applications extend to the study of biochemical pathways and the design of enzyme inhibitors.

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