Home Chemistry Organic Building Blocks Aryls 1,3,4,5-Tetrahydro-2H-Benzo[B]Azepin-2-One
Hydrolysis: The lactam ring (the -2-one part) can be hydrolyzed to form a carboxylic acid.
Reduction: The double bond in the azepin ring could potentially be reduced.
Acylation: The amine group (NH) can be acylated to form amide derivatives.
Oxidation: The compound can potentially undergo various oxidation reactions, particularly at sites containing hydrogen atoms.
Halogenation: The compound can be halogenated at suitable sites if appropriate reagents are used.
Substitution reactions: Various functional group substitutions can occur, depending on the conditions and reagents used.
Cyclization reactions: Depending on the reaction conditions and available functional groups, intramolecular cyclization reactions may occur.
Metal-catalyzed reactions: Reactions involving transition metal catalysts can lead to various transformations, such as C-C bond formation or other functional group interconversions.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Carbon related+−
Formula Weight+−
click to sign in and save
8-Methoxy-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
8-Amino-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
7-Methoxy-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
6-Fluoro-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
6-Bromo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
3-Bromo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
(S)-3-Amino-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
click to sign in and save
tert-Butyl 2-(3-amino-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetate
click to sign in and save
2-(3-((tert-Butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid
click to sign in and save
3-Chloro-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :