10-Hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

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Reagent Code: #195572
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CAS Number 29331-92-8

science Other reagents with same CAS 29331-92-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.28 g/mol
Formula C₁₅H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD00871817
thermostat Physical Properties
Boiling Point 431.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as an intermediate in the synthesis of certain anticonvulsant and mood-stabilizing medications. It plays a key role in the production of drugs targeting neurological disorders such as epilepsy and bipolar disorder. Due to its structural similarity to dibenzazepine derivatives, it contributes to the development of compounds that modulate sodium channels in nerve cells, helping regulate abnormal electrical activity in the brain. Its hydroxyl and carboxamide functional groups allow for further chemical modifications, making it valuable in pharmaceutical research and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,150.00
inventory 250mg
10-20 days ฿1,720.00
inventory 5g
10-20 days ฿17,500.00
inventory 1g
10-20 days ฿4,120.00

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10-Hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide
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Used primarily as an intermediate in the synthesis of certain anticonvulsant and mood-stabilizing medications. It plays a key role in the production of drugs targeting neurological disorders such as epilepsy and bipolar disorder. Due to its structural similarity to dibenzazepine derivatives, it contributes to the development of compounds that modulate sodium channels in nerve cells, helping regulate abnormal electrical activity in the brain. Its hydroxyl and carboxamide functional groups allow for furthe

Used primarily as an intermediate in the synthesis of certain anticonvulsant and mood-stabilizing medications. It plays a key role in the production of drugs targeting neurological disorders such as epilepsy and bipolar disorder. Due to its structural similarity to dibenzazepine derivatives, it contributes to the development of compounds that modulate sodium channels in nerve cells, helping regulate abnormal electrical activity in the brain. Its hydroxyl and carboxamide functional groups allow for further chemical modifications, making it valuable in pharmaceutical research and development.

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