CAS 1713-33-3

1-methyl-7-oxabicyclo[4.1.0]heptane

Description:

1-Methyl-7-oxabicyclo[4.1.0]heptane, with the CAS number 1713-33-3, is a bicyclic organic compound characterized by its unique bicyclic structure that includes a seven-membered ring with an oxygen atom incorporated into the framework. This compound features a methyl group attached to one of the carbon atoms in the bicyclic system, influencing its chemical properties and reactivity. The presence of the oxygen atom contributes to its potential as a functional group, which may participate in various chemical reactions, including nucleophilic attacks or hydrogen bonding. The bicyclic nature of the compound can impart rigidity to its structure, affecting its physical properties such as boiling point, melting point, and solubility. Additionally, the compound may exhibit interesting stereochemistry due to the arrangement of its substituents, which can influence its interactions in biological systems or its utility in synthetic chemistry. Overall, 1-methyl-7-oxabicyclo[4.1.0]heptane is a compound of interest in organic synthesis and may have applications in medicinal chemistry or materials science.

Formula: C₇H₁₂O

InChI: InChI=1/C7H12O/c1-7-5-3-2-4-6(7)8-7/h6H,2-5H2,1H3/t6-,7+/m1/s1

Synonyms:

• 1,2-Epoxy-1-methylcyclohexane
• 1-Methyl-1,2-epoxycyclohexane
• (1S,6R)-1-methyl-7-oxabicyclo[4.1.0]heptane

1-Methyl-1,2-epoxycyclohexane

CAS: 1713-33-3

Formula: C₇H₁₂O

Purity: >95.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 112.17

Ref: 3B-M1983

1-methyl-7-oxabicyclo[4.1.0]heptane

CAS: 1713-33-3

Formula: C₇H₁₂O

Purity: 96%

Color and Shape: Liquid

Molecular weight: 112.1696

Ref: IN-DA003EIG

1,2-Epoxy-1-methylcyclohexane

CAS: 1713-33-3

1,2-Epoxy-1-methylcyclohexane

Purity: 97%

Molecular weight: 112.17g/mol

Ref: 54-OR939738

1,2-Epoxy-1-methyl-cyclohexane

CAS: 1713-33-3

1,2-Epoxy-1-methylcyclohexane is a nucleophile that is useful for the synthesis of epoxides. It is a bifunctional compound that can be used as an asymmetric synthesis catalyst. 1,2-Epoxy-1-methylcyclohexane has been shown to react with urea derivatives to form epoxides through reductive elimination. This reaction also produces cyclopentene oxide as a byproduct. The selectivity of this reaction depends on the temperature and acidic conditions used in the reaction. 1,2-Epoxy-1-methylcyclohexane has significant homology with other epoxides and epoxide derivatives. Epoxides are organic compounds with two hydrocarbons covalently bonded by one oxygen atom. Epoxides are typically produced from alkenes and are classified into three groups: simple (single bond), ethylenic (double bond), and cyclic (three or more bonds).

Formula: C₇H₁₂O

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 112.17 g/mol

Ref: 3D-FE172342

1,2-Epoxy-1-methylcyclohexane

CAS: 1713-33-3

Purity: 96%

Color and Shape: Liquid

Molecular weight: 112.1719971

Ref: 10-F692693