benzyl 4-broMo-3-(1-hydroxyethyl)-5,6-dihydropyridine-1(2H)-carboxylate

97%(HPLC)

Reagent Code: #50811
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CAS Number 1823808-97-4

science Other reagents with same CAS 1823808-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.21 g/mol
Formula C₁₅H₁₈BrNO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a bromo group and a hydroxyl group, makes it a versatile building block for constructing pharmacologically active compounds. Researchers often employ it in the development of potential drug candidates, particularly in the creation of molecules with therapeutic properties targeting neurological disorders or infections. Additionally, its dihydropyridine core is of interest in medicinal chemistry for designing compounds that interact with calcium channels, which are critical in cardiovascular and neurological research. The compound’s functional groups also allow for further chemical modifications, enabling its use in the synthesis of diverse chemical libraries for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00
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benzyl 4-broMo-3-(1-hydroxyethyl)-5,6-dihydropyridine-1(2H)-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a bromo group and a hydroxyl group, makes it a versatile building block for constructing pharmacologically active compounds. Researchers often employ it in the development of potential drug candidates, particularly in the creation of molecules with therapeutic properties targeting neurological disorders or infections. Additionally, its dihydropyridine core is of interest in medicinal chemistry for designing compounds that interact with calcium channels, which are critical in cardiovascular and neurological research. The compound’s functional groups also allow for further chemical modifications, enabling its use in the synthesis of diverse chemical libraries for drug discovery and development.
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