Chemical properties of oxetane compounds:
1.Ring-opening reaction.
Catalyzed by an acid or base, oxetane compounds can undergo a ring-opening reaction to produce the corresponding alcohol or ether. For example, 2-methyl-2-oxetane is annuluciferized under acidic conditions to form isopropyl ether. The mechanism of the ring-opening reaction is that the carbon-oxygen bond of the oxetane compound is broken under the action of acid or base to form the corresponding carbocation or carboanion, which is then combined with water or alcohol to form the corresponding alcohol or ether.
2.Properties of ethylene oxide.
Oxetane compounds have the properties of ethylene oxide, such as aromatic nucleophilic substitution reaction and double bond oxidation reaction. Due to the presence of ring tension in oxetane compounds, they are highly reactive and can react with a wide variety of nucleophiles. For example, under acidic conditions, oxetane compounds can be hydrolyzed with water to produce the corresponding alcohol; Under alkaline conditions, it can undergo substitution reaction with alcohol to form ether. In addition, oxetane compounds can also react with nucleophiles such as amino and sulfhydryl groups.
Product Information] Name: Oxetane compound.
Purity: 95%+
Retention time: 1 year.
Specification: mg g
Packing: bottled and bagged.
Storage conditions: -20°C in the dark.
Uses: Only for scientific research, not for human body.
Manufacturer: Xi'an Haoran Biotechnology.
Related products: 2-Alkoxy-1,2-oxobon hetepentacyclic.
5-propylbenzo1,3-dioxane.
1,4,7,10,13,16-Hexaoxacyclooctadecane.
5-propylbenzo1,3-dioxane.
Oxygen cups[4] aromatic hydrocarbons.
Tetraoxane cups[2]aromatic hydrocarbons[2]triazine.
Azavia[2]carbazole[2]aromatics.
The above information comes from Haoran MSQ2024.2.26