Home Chemistry Heterocyclic Building Blocks Benzoxazoles 3-Phenylbenzo[D]Oxazol-3-Ium
Nucleophilic Substitution: The pyrazole ring can undergo nucleophilic substitution reactions at its carbon atoms. For example, you can react it with alkyl halides to substitute the halogen atom with the pyrazole ring.
Acylation: It can undergo acylation reactions, where an acyl group is added to the nitrogen atom of the pyrazole ring. This can be achieved using acyl chlorides or anhydrides in the presence of a base.
Reduction: Reduction reactions can be performed on the pyrazole ring to convert it to a tetrahydro-2H-pyran-substituted piperidine ring or related structures. Common reducing agents like sodium borohydride or lithium aluminum hydride can be used.
Ring-Opening: The tetrahydro-2H-pyran ring can be opened under acidic or basic conditions, leading to the formation of open-chain compounds.
Cyclization: Depending on the reaction conditions and reagents, you can induce cyclization reactions to form other heterocyclic compounds, especially if there are additional functional groups on the molecule.
Oxidation: The compound can undergo oxidation reactions if suitable oxidizing agents are used. This can lead to the formation of various oxidized derivatives.
Cross-Coupling Reactions: If there are appropriate functional groups present (e.g., halides or boronic acids), you can perform cross-coupling reactions like Suzuki-Miyaura or Heck reactions to introduce other substituents.
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5,7-Di-tert-butyl-3-(4-(trifluoromethyl)phenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(4-chlorophenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(3,4-dichlorophenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(3-fluorophenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(4-(trifluoromethoxy)phenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(4-methoxyphenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-phenylbenzo[d]oxazol-3-ium tetrafluoroborate
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5,7-Di-tert-butyl-3-(3,5-dimethylphenyl)benzo[d]oxazol-3-ium tetrafluoroborate
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