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CS-W001157 4
Total: USD 88.00

1,2-Epoxy-1-methylcyclohexane

  • CAS No. 1713-33-3

  • Cat. No. CS-0152704
  • Purity≥95%
  • MDL No.MFCD11846121

*For research and further manufacturing use only, not for direct human use.

1,2-Epoxy-1-methylcyclohexane|CS-0152704

Structure of 1713-33-3

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General Information

  • CAS No. 1713-33-3
  • Cat. No. CS-0152704
  • Purity ≥95%
  • MDL No. MFCD11846121
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₂O
  • Molecular Weight 112.17
  • Synonym(s) 1-Methyl-7-oxabicyclo[4.1.0]heptane
  • SMILES CC12CCCCC1O2

Description

1,2-Epoxy-1-methylcyclohexane is a strained epoxide featuring a tertiary carbon adjacent to the oxirane ring, enhancing its reactivity in nucleophilic ring-opening reactions. This bench-stable, moisture-tolerant cyclic ether integrates readily into synthetic pathways requiring stereocontrolled functionalization, particularly in the construction of complex carbocyclic frameworks under mild conditions.

Application

1,2-Epoxy-1-methylcyclohexane serves as a versatile chiral epoxide building block in synthetic organic chemistry. Its strained three-membered ring enables regioselective ring-opening reactions with nucleophiles under mild conditions, facilitating the construction of complex oxygenated scaffolds. The molecule exhibits good bench stability and compatibility with diverse functional groups, enabling straightforward incorporation into multi-step syntheses. Its well-defined stereochemistry supports stereoselective transformations, making it valuable for the preparation of natural product intermediates and functionalized cyclohexane derivatives.

Safety Information

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GHS Pictogram :
GHS No : GHS02,GHS07
Signal Word : Danger
UN#: 1993
Class : 3
Packing Group : Ⅲ
Hazard Statements : H226-H315-H319
Precautionary Statements : P210-P233-P240-P241-P242-P243-P264-P280-P302+P352-P303+P361+P353-P305+P351+P338-P332+P313-P337+P313-P362+P364-P370+P378-P403+P235-P501

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Computational Chemistry Data

  • TPSA   12.53
  • LogP   1.7179
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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