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

97%

Reagent Code: #219574
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CAS Number 939986-23-9

science Other reagents with same CAS 939986-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.36 g/mol
Formula C₁₅H₂₂N₄O₄
badge Registry Numbers
MDL Number MFCD09607535
inventory_2 Storage & Handling
Density 1.24 g/cm3
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 carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿17,300.00
(3´-Nitro-3,4,5,6-tetrahydro-2H-[1,2´]bipyridinyl-3-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 carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

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 carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

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