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Structure of 2416-94-6
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2,3,6-Trimethylphenol features a sterically hindered aromatic ring stabilized by three methyl groups, enhancing resistance to oxidation and facilitating selective functionalization. This bench-stable phenolic scaffold serves as a robust building block in synthetic organic chemistry and materials development.
2,3,6-Trimethylphenol serves as a versatile building block in synthetic organic chemistry, offering enhanced steric and electronic properties due to its three methyl substituents. Its stability under standard reaction conditions facilitates use in electrophilic aromatic substitution, coupling reactions, and the construction of functionalized heterocycles. The compound functions effectively as a precursor in the synthesis of agrochemicals, pharmaceutical intermediates, and specialty polymers, with predictable reactivity and ease of purification.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H317-H318
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: