Home Chemistry Heterocyclic Building Blocks Triazines 2,4,6-Triphenoxy-1,3,5-Triazine
Amination: You can introduce amino groups into the molecule by using suitable aminating agents, such as ammonia or amine derivatives. This can lead to the formation of 2,4,6-triamino-1,3,5-triazine derivatives.
Halogenation: The compound can undergo halogenation reactions, where one or more of the phenoxy groups can be replaced with halogen atoms (e.g., chlorine or bromine) by using halogenating agents like chlorine or bromine.
Acylation: You can introduce acyl groups into the molecule using acylating agents like acyl chlorides or anhydrides, leading to the formation of acylated derivatives.
Reduction: Reduction reactions can be employed to reduce the nitrogens in the triazine ring or to reduce any functional groups present in the phenoxy substituents. Common reducing agents include hydrazine or metal catalysts.
Oxidation: Depending on the reaction conditions, the compound can undergo oxidation reactions to form products with different oxidation states.
Cross-Coupling Reactions: If you have functional groups suitable for cross-coupling reactions (e.g., aryl halides), you can perform reactions like Suzuki-Miyaura coupling or Heck coupling to attach other aryl groups or organic moieties to the triazine ring.
Hydrolysis: The phenoxy groups in the molecule can undergo hydrolysis reactions when exposed to strong acidic or basic conditions, leading to the cleavage of the ether bonds and the formation of corresponding phenols or phenolate salts.
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2,4,6-Tris(2,4,6-tribromophenoxy)-1,3,5-triazine
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4,4',4''-((1,3,5-Triazine-2,4,6-triyl)tris(oxy))tribenzoic acid
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4,4',4''-((1,3,5-Triazine-2,4,6-triyl)tris(oxy))trianiline
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4,4',4''-((1,3,5-Triazine-2,4,6-triyl)tris(oxy))tribenzaldehyde
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