Home Chemistry Organic Building Blocks Aryls (6-Phenoxytetrahydro-2H-Pyran-2-Yl)Methanol
Ether Cleavage: The phenoxy group is an ether, and it could potentially undergo cleavage reactions under acidic or basic conditions, yielding a phenol and an alcohol
Oxidation Reactions: The benzylic carbon in the phenoxy group is susceptible to oxidation. Oxidizing agents could convert the alcohol into a carbonyl compound (aldehyde or ketone).
Acetal Formation: The alcohol group could react with carbonyl compounds to form acetals, especially under acidic conditions.
Reduction Reactions: The carbonyl group in the tetrahydro-2H-pyran ring could undergo reduction to form the corresponding alcohols
Nucleophilic Substitution: The hydroxyl group can act as a nucleophile and undergo substitution reactions with appropriate electrophiles, like alkyl halides or tosylates.
Esterification: The alcohol group can undergo esterification reactions with carboxylic acids or acid chlorides to form ester.
Protecting Group Formation: The alcohol group could be used as a protecting group for other reactive functional groups in a synthesis.
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2-Chloro-4-nitrophenyl β-D-glucopyranoside
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