Home Chemistry Heterocyclic Building Blocks Triazoles 1-Phenethyl-1H-1,2,4-Triazole
Amination: Amination reactions can be carried out to introduce amino groups (-NH2) to the molecule. This can be done by reacting it with appropriate aminating agents.
Oxidation: 1-Phenethyl-1H-1,2,4-triazole may be susceptible to oxidation under certain conditions, leading to the formation of oxidized products.
Reduction: Reduction reactions can be used to reduce functional groups within the molecule, such as converting nitro groups (-NO2) to amino groups (-NH2).
Halogenation: Halogenation reactions can be used to introduce halogen atoms (e.g., chlorine, bromine) into the molecule.
Substitution reactions: The phenethyl group or hydrogen atoms on the triazole ring can undergo substitution reactions, where one group is replaced by another.
Cyclization: Depending on the reaction conditions and reagents, 1-Phenethyl-1H-1,2,4-triazole may undergo intramolecular cyclization reactions, forming new cyclic compounds.
Hydrolysis: Under certain conditions, the compound may undergo hydrolysis reactions, where chemical bonds are broken by water, leading to the formation of different products.
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(2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanoic acid
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(2R,3R)-2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
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(2S,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile
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(2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanamide
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(2R,3R)-2-(2,5-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol
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(2R,3R)-2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol
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