Home Chemistry Heterocyclic Building Blocks Indoles (1H-Indol-2-Yl)Methanol
Oxidation Reactions: The alcohol group in can be oxidized to the corresponding aldehyde or carboxylic acid under the appropriate conditions. Common oxidizing agents include chromates, permanganates, and various metal catalysts.
Esterification: The alcohol group can undergo esterification reactions with carboxylic acids or acid chlorides to form esters.
Nucleophilic Substitution: The indole nitrogen can act as a nucleophile and participate in nucleophilic substitution reactions with electrophiles. For example, it might react with alkyl halides or sulfonyl chlorides.
Reduction: The indole ring or the carbonyl group can be reduced under certain conditions. For example, the alcohol group may be reduced to a hydrocarbon or the indole ring reduced to dihydroindole.
Acetylation: The alcohol group can be acetylated using acetic anhydride or acetyl chloride to form the corresponding acetateester
Condensation Reactions: (1H-indol-2-yl)methanol can undergo condensation reactions with suitable reactants to form various heterocyclic compounds.
Grignard Reaction: The indole nitrogen or the alcohol group can potentially react with a Grignard reagent to form more complex products.
Diazo Coupling: The indole nitrogen can participate in diazo coupling reactions, forming azo compounds.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :