(3´-Nitro-3,4,5,6-tetrahydro-2H-[1,2´]bipyridinyl-4-yl)-carbamicacidtert-butylester

97%

Reagent Code: #219625
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CAS Number 833452-36-1

science Other reagents with same CAS 833452-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.36 g/mol
Formula C₁₅H₂₂N₄O₄
badge Registry Numbers
MDL Number MFCD09607541
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl ester group allows for selective deprotection, enabling stepwise construction of complex molecules in medicinal chemistry. Commonly employed in solid-phase and solution-phase synthesis due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,410.00
(3´-Nitro-3,4,5,6-tetrahydro-2H-[1,2´]bipyridinyl-4-yl)-carbamicacidtert-butylester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl ester group allows for selective deprotection, enabling stepwise construction of complex molecules in medicinal chemistry. Commonly employed in solid-phase and solution-phase synthesis du

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl ester group allows for selective deprotection, enabling stepwise construction of complex molecules in medicinal chemistry. Commonly employed in solid-phase and solution-phase synthesis due to its stability and reactivity profile.

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