Home Chemistry Heterocyclic Building Blocks Isoxazoles 5-Cyclopropylisoxazole
Ring Opening Reactions: The cyclopropyl ring in 5-cyclopropylisoxazole is strained and can undergo ring-opening reactions, such as nucleophilic ring opening, to form products with an open chain.
Nucleophilic Substitution: The nitrogen atom in the isoxazole ring can act as a nucleophile, undergoing substitution reactions with electrophiles, such as alkyl halides or acyl chlorides.
Electrophilic Aromatic Substitution: If there are electron-rich substituents on the isoxazole ring, it can undergo electrophilic aromatic substitution reactions with electrophiles, such as nitration, halogenation, or Friedel-Crafts reactions.
Oxidation and Reduction: Depending on the reaction conditions, 5-cyclopropylisoxazole can undergo oxidation or reduction reactions. For example, it can be oxidized to form corresponding isoxazole-4-carboxylic acid or reduced to form isoxazolidine derivatives.
Cyclization Reactions: The compound may participate in intramolecular cyclization reactions, leading to the formation of various cyclic products.
Heterocyclic Chemistry: Given its isoxazole ring, it can participate in various heterocyclic chemistry reactions, such as Diels-Alder reactions with suitable dienophiles.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
tert-Butyl (1-(4-bromo-3-methylisoxazol-5-yl)cyclopropyl)carbamate
click to sign in and save
5-Cyclopropylisoxazole-4-carboxylic acid
click to sign in and save
1-(4-Bromo-3-methylisoxazol-5-yl)cyclopropane-1-carboxylic acid
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :