1aH-Dibenzo[b,f]oxireno[2,3-d]azepine-6(10bH)-carboxamide

Analytical reference substance, ≥98% (HPLC)

Reagent Code: #158182
label
Alias Carbamazepine 10,11-epoxide
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CAS Number 36507-30-9

science Other reagents with same CAS 36507-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.27 g/mol
Formula C₁₅H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD00467137
thermostat Physical Properties
Melting Point 204-206 °C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in research as a key intermediate for synthesizing bioactive compounds targeting central nervous system disorders. Shows potential in the development of anticonvulsant and neuroprotective agents due to its structural similarity to tricyclic compounds with known neurological activity. Investigated for its interaction with GABA receptors and related neurotransmitter systems. Also explored in the design of novel anti-inflammatory agents where modulation of neuronal inflammation is required. Not used in consumer products; strictly limited to laboratory and pharmaceutical research settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿3,380.00
inventory 25mg
10-20 days ฿14,000.00

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1aH-Dibenzo[b,f]oxireno[2,3-d]azepine-6(10bH)-carboxamide
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Used in research as a key intermediate for synthesizing bioactive compounds targeting central nervous system disorders. Shows potential in the development of anticonvulsant and neuroprotective agents due to its structural similarity to tricyclic compounds with known neurological activity. Investigated for its interaction with GABA receptors and related neurotransmitter systems. Also explored in the design of novel anti-inflammatory agents where modulation of neuronal inflammation is required. Not used in

Used in research as a key intermediate for synthesizing bioactive compounds targeting central nervous system disorders. Shows potential in the development of anticonvulsant and neuroprotective agents due to its structural similarity to tricyclic compounds with known neurological activity. Investigated for its interaction with GABA receptors and related neurotransmitter systems. Also explored in the design of novel anti-inflammatory agents where modulation of neuronal inflammation is required. Not used in consumer products; strictly limited to laboratory and pharmaceutical research settings.

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