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

97%(HPLC)

Reagent Code: #50547
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CAS Number 1823268-14-9

science Other reagents with same CAS 1823268-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.2 g/mol
Formula C₁₅H₁₆BrNO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique structure, featuring both a benzyl group and a bromo substituent, makes it a valuable building block in the synthesis of pharmaceuticals, particularly in the creation of heterocyclic compounds. The presence of the acetyl group allows for further functionalization, enabling the production of targeted molecules with potential biological activity. Additionally, it is often employed in medicinal chemistry research for the design and optimization of drug candidates, particularly those targeting neurological or inflammatory pathways. Its role in facilitating the construction of diverse molecular frameworks underscores its importance in the field of 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 3-acetyl-4-broMo-5,6-dihydropyridine-1(2H)-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique structure, featuring both a benzyl group and a bromo substituent, makes it a valuable building block in the synthesis of pharmaceuticals, particularly in the creation of heterocyclic compounds. The presence of the acetyl group allows for further functionalization, enabling the production of targeted molecules with potential biological activity. Additiona

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique structure, featuring both a benzyl group and a bromo substituent, makes it a valuable building block in the synthesis of pharmaceuticals, particularly in the creation of heterocyclic compounds. The presence of the acetyl group allows for further functionalization, enabling the production of targeted molecules with potential biological activity. Additionally, it is often employed in medicinal chemistry research for the design and optimization of drug candidates, particularly those targeting neurological or inflammatory pathways. Its role in facilitating the construction of diverse molecular frameworks underscores its importance in the field of drug discovery and development.

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