5-(4-Boc-piperazino)-2-nitroanisole

98%

Reagent Code: #86186
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CAS Number 1017782-79-4

science Other reagents with same CAS 1017782-79-4

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Weight 337.37 g/mol
Formula C₁₆H₂₃N₃O₅
badge Registry Numbers
MDL Number MFCD09972251
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description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. The Boc (tert-butoxycarbonyl) protecting group on the piperazine moiety allows for selective reactions to be carried out on other parts of the molecule, making it valuable in multi-step synthetic processes. Additionally, the nitro and methoxy groups provide reactive sites for further functionalization, enabling the creation of diverse chemical structures. Its role in medicinal chemistry includes the synthesis of drug candidates targeting various biological pathways, such as central nervous system disorders or infectious diseases.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,391.00
inventory 5g
10-20 days ฿16,380.00

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5-(4-Boc-piperazino)-2-nitroanisole
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This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. The Boc (tert-butoxycarbonyl) protecting group on the piperazine moiety allows for selective reactions to be carried out on other parts of the molecule, making it valuable in multi-step synthetic processes. Additionally, the nitro and methoxy groups p

This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. The Boc (tert-butoxycarbonyl) protecting group on the piperazine moiety allows for selective reactions to be carried out on other parts of the molecule, making it valuable in multi-step synthetic processes. Additionally, the nitro and methoxy groups provide reactive sites for further functionalization, enabling the creation of diverse chemical structures. Its role in medicinal chemistry includes the synthesis of drug candidates targeting various biological pathways, such as central nervous system disorders or infectious diseases.

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