3-Nitro-10,11-dihydro-5H-dibenzo[b,f]azepine

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Reagent Code: #219254
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CAS Number 79752-06-0

science Other reagents with same CAS 79752-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.26 g/mol
Formula C₁₄H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD30471816
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of tricyclic antidepressants. Its structure serves as a key building block for modifying bioactive molecules targeting the central nervous system. It is also employed in research settings for exploring new psychoactive substances and studying structure-activity relationships in azepine derivatives. Due to the nitro group, it can undergo reduction to form amino derivatives, which are valuable in further chemical transformations for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,210.00
inventory 250mg
10-20 days ฿46,670.00

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3-Nitro-10,11-dihydro-5H-dibenzo[b,f]azepine
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of tricyclic antidepressants. Its structure serves as a key building block for modifying bioactive molecules targeting the central nervous system. It is also employed in research settings for exploring new psychoactive substances and studying structure-activity relationships in azepine derivatives. Due to the nitro group, it can undergo reduction to form amino derivatives, which are valuable in

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of tricyclic antidepressants. Its structure serves as a key building block for modifying bioactive molecules targeting the central nervous system. It is also employed in research settings for exploring new psychoactive substances and studying structure-activity relationships in azepine derivatives. Due to the nitro group, it can undergo reduction to form amino derivatives, which are valuable in further chemical transformations for drug discovery.

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