187601-84-9

Basic information

• Product Name: 8-methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one
• Synonyms: 8-methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one
• CAS NO: 187601-84-9
• Molecular Formula: C11H13NO2
• Molecular Weight: 191
• Mol File: 187601-84-9.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 8-methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 8-methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one(187601-84-9)
• EPA Substance Registry System: 8-methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one(187601-84-9)

Safety Data

• Hazardous Substances Data: 187601-84-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
8-Methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one is used as an antiepileptic medication for the treatment of partial seizures. It is prescribed due to its ability to inhibit the spread of seizure activity in the brain, providing relief to patients suffering from epilepsy.
Used in Neurological Treatment:
Oxcarbazepine is utilized as a therapeutic agent in the management of neurological conditions characterized by seizures. Its efficacy in controlling seizure activity makes it a valuable component in the treatment plans for individuals with epilepsy.
Used in Drug Development Research:
As a prodrug, 8-Methoxy-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one is also used in research for the development of new antiepileptic drugs. Its metabolism and mechanism of action provide insights into the design of potentially more effective or safer medications for seizure disorders.

Upstream product

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Relevant articles and documents

HETEROCYCLIC ACYL HYDRAZONE LINKERS, METHODS AND USES THEREOF

The present application is directed to compounds of Formula (I): compounds of Formula (II): compounds of Formula (III): and compounds of Formula (IV): compositions comprising these compounds and their uses, for example as medicaments and /or diagnostics.

Azabenzocycloheptenones. Part 20. Synthesis and utilisation of 4-amino-1,2,3,4-tetrahydro-1(1H)-benzazepines

1,2,3,4-Tetrahydro-6- and -7-methoxy-4-oxo-1-(p-tolylsulfonyl)quinolines 3 (R = tosyl, X = 6- and 7-OMe) and 1-ethoxycarbonylmethyl-1,2,3,4-tetrahydro-7-methoxy-4-oxoquinoline3 (R = CH2CO2Et, X = 7-OMe) have been ring-expanded in two