Home Chemistry Heterocyclic Building Blocks Aliphatic Heterocycles 1,2-Dithiolane
Ambeed provide 1 derivatives of 1,2-dithiolane.
Oxidation: 1,2-Dithiolane can be oxidized to form the corresponding sulfoxide or sulfone. This oxidation can be achieved using oxidizing agents such as hydrogen peroxide or peracids.
Ring Opening: 1,2-Dithiolane can undergo ring-opening reactions under certain conditions. For example, treatment with strong bases can lead to the cleavage of the ring, forming thiol and alcohol or other products.
Alkylation: The carbon atom in the 1,2-dithiolane ring can be alkylated with alkyl halides in the presence of a base. This reaction results in the formation of alkylated dithiolane derivatives.
Acylation: 1,2-Dithiolane can undergo acylation reactions with acyl chlorides or anhydrides in the presence of a base or catalyst. This leads to the formation of acylated dithiolane compounds.
Reduction: The sulfur atoms in the dithiolane ring can be reduced to thiol groups using reducing agents like sodium borohydride.
Disulfide Formation: 1,2-Dithiolane can be oxidized to form disulfide compounds. This reaction can occur under oxidative conditions.
Addition Reactions: Depending on the reactants and conditions, 1,2-dithiolane can undergo various addition reactions, including reactions with electrophiles or nucleophiles.
Substitution Reactions: Substitution reactions can occur at the carbon atom in the 1,2-dithiolane ring when appropriate reactants are used.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
Dimethyl 2-(1,2-dithiolan-3-yl)malonate
click to sign in and save
4-Methyl-1,2-dithiolane-4-carboxylic acid
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :