Home Chemistry Heterocyclic Building Blocks Oxazines Spiro[Benzo[D][1,3]Oxazine-4,4'-Piperidin]-2(1H)-One
Hydrolysis: The amide group in the piperidin-2-one moiety can undergo hydrolysis in acidic or basic conditions to produce the corresponding carboxylic acid or amine, respectively.
Reductive reactions: Reduction of the carbonyl group in the piperidin-2-one ring can be achieved using reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Nucleophilic substitution: Depending on the substituents present, nucleophilic substitution reactions can take place at various positions within the molecule.
Cyclization reactions: The compound's unique spiro structure can potentially undergo intramolecular cyclization reactions under suitable conditions.
Functional group transformations: Different functional groups present in the molecule, such as alcohols, amines, or halides, can undergo various chemical transformations, including esterification, amidation, or halogenation.
Oxidation reactions: The compound can be oxidized using various oxidizing agents to convert functional groups or to modify the structure.
Reactions with electrophiles: Depending on the reactivity of the compound, it may react with electrophiles to form adducts or products.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
tert-Butyl 6-chloro-2-oxo-1,2-dihydrospiro[benzo[d][1,3]oxazine-4,4'-piperidine]-1'-carboxylate
click to sign in and save
6-Fluorospiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-one
click to sign in and save
6-Chloro-1,2-dihydro-2-oxospiro[4H-3,1-benzoxazin-4,4'-piperidine]
click to sign in and save
1'-Boc-1,2-dihydro-2-oxo-spiro[4H-3,1-benzoxazine-4,4'-piperidine]
click to sign in and save
Spiro[benzo[d][1,3]oxazine-4,4'-piperidin]-2(1H)-one hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :