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CAS 130232-97-2

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(2S)-2-[(1,1-Dimethylethoxy)methyl]oxirane

Description:
(2S)-2-[(1,1-Dimethylethoxy)methyl]oxirane, also known as a chiral epoxide, is characterized by its three-membered cyclic ether structure, which includes an oxygen atom and two carbon atoms. The presence of the (2S) configuration indicates that it has specific stereochemistry, which can influence its reactivity and interactions with biological systems. The dimethylethoxy group contributes to its hydrophobic characteristics, potentially affecting its solubility and reactivity in various solvents. Epoxides are known for their high reactivity due to the strained ring structure, making them useful intermediates in organic synthesis, particularly in the formation of alcohols, amines, and other functional groups through ring-opening reactions. This compound may also exhibit unique properties in terms of its biological activity, depending on its stereochemistry and functional groups. Overall, (2S)-2-[(1,1-Dimethylethoxy)methyl]oxirane is a valuable compound in synthetic organic chemistry and may have applications in pharmaceuticals and materials science.
Formula:C7H14O2
InChI:InChI=1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3/t6-/m0/s1
InChI key:InChIKey=SFJRUJUEMVAZLM-LURJTMIESA-N
SMILES:C(OC(C)(C)C)[C@@H]1CO1
Synonyms:
  • (+)-tert-Butyl glycidyl ether
  • (2S)-2-(tert-Butoxymethyl)oxirane
  • (2S)-2-[(1,1-Dimethylethoxy)methyl]Oxirane
  • (2S)-2-[(2-Methylpropan-2-yl)oxymethyl]oxirane
  • Oxirane, [(1,1-dimethylethoxy)methyl]-, (+)-
  • Oxirane, [(1,1-dimethylethoxy)methyl]-, (2S)-
  • oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S)-
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