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CAS 106268-96-6

:

(R)-(-)-2-Methylglycidyl 4-nitrobenzoate

Description:
(R)-(-)-2-Methylglycidyl 4-nitrobenzoate is an organic compound characterized by its chiral structure, which includes a glycidyl group and a nitrobenzoate moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its reactivity due to the presence of the epoxide group, which can undergo ring-opening reactions in the presence of nucleophiles. The nitrobenzoate portion contributes to its polar characteristics, enhancing solubility in various organic solvents. This compound is often utilized in synthetic organic chemistry, particularly in the preparation of more complex molecules, and may serve as an intermediate in the synthesis of pharmaceuticals or agrochemicals. Its chiral nature allows for potential applications in asymmetric synthesis, where the specific enantiomer can influence the biological activity of the resulting compounds. Safety data should be consulted, as it may pose hazards typical of organic compounds, including flammability and potential toxicity.
Formula:C11H11NO5
InChI:InChI=1S/C11H11NO5/c1-11(7-17-11)6-16-10(13)8-2-4-9(5-3-8)12(14)15/h2-5H,6-7H2,1H3/t11-/m0/s1
InChI key:InChIKey=PUBTVFBOTFDPTA-NSHDSACASA-N
SMILES:C(OC(=O)C1=CC=C(N(=O)=O)C=C1)[C@@]2(C)CO2
Synonyms:
  • (2R)-(-)-(2,3-Epoxy-2-Methylpropylester)-4-Nitrobenzoate
  • (R)-(-)-2-Methylglycidyl 4-nitrobenzoate
  • (R)-(2-Methyloxiran-2-yl)methyl 4-nitrobenzoate
  • 2,3-Epoxy-2-Methylpropylester-4-Nitrobenzoate
  • 2-Methylglycidyl 4-Nitrobenzoate
  • 2-Oxiranemethanol, 2-methyl-, 2-(4-nitrobenzoate), (2R)-
  • 3-Methyl-,4-Nitrobenzoate,(R)-Oxiranemethano
  • Oxiranemethanol, 2-methyl-, 4-nitrobenzoate, (2R)-
  • Oxiranemethanol, 2-methyl-, 4-nitrobenzoate, (R)-
  • [(2R)-3-methyloxiran-2-yl]methyl 4-nitrobenzoate
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