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Structure of 129228-11-1
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This sterically hindered alkane features two methoxymethyl groups flanking a central carbon, enhancing solubility in polar organic solvents. The dimethyl substitution stabilizes the backbone against oxidative degradation, enabling use under standard bench conditions. This scaffold serves as a robust hydrophobic core for probing steric effects in medicinal chemistry and materials design.
3,3-Bis(methoxymethyl)-2,6-dimethylheptane serves as a stable, bench-friendly building block for the synthesis of complex terpene-like scaffolds and functionalized cyclohexane derivatives. Its geminal bis(alkoxy) functionality enables selective deprotection and transformation under mild acidic conditions, while the alkyl framework provides steric bulk and compatibility with standard coupling reactions. Functions effectively in multi-step syntheses requiring orthogonal protection strategies.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H302
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: