4,8-di(thiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-Thiophenes| Ambeed

: Hydrolysis: The Schiff base can undergo hydrolysis in the presence of acid or base to yield the corresponding amine and ketone. Reduction: The imine group can be reduced to the corresponding amine using reducing agents like sodium borohydride (NaBH₄) or lithium aluminum hydride (LiAlH₄). Mannich Reaction: The compound can react with amines and formaldehyde to form Mannich adducts, which are β-amino carbonyl compounds. Condensation Reactions: It can participate in condensation reactions with various nucleophiles, including alcohols and amines, to form new carbon-nitrogen or carbon-oxygen bonds. Acylation: The carbonyl group can undergo acylation reactions with acyl chlorides or anhydrides to form amides. Oxidation: The compound can be oxidized to form indole derivatives or other products, depending on the reaction conditions and reagents used. Reductive Amination: The Schiff base can be used as a starting material for reductive amination reactions, where it reacts with an amine and a reducing agent to form secondary or tertiary amines.

$39.00/10mg