1195-92-2 | 7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(1-methylethenyl)-

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$61.00	$43.00
5g	95%	in stock	$187.00	$131.00
25g	95%	in stock	$605.00	$423.00

Description

• Catalog Number: AA24288
• Chemical Name: 7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(1-methylethenyl)-
• CAS Number: 1195-92-2
• Molecular Formula: C10H16O
• Molecular Weight: 152.2334
• MDL Number: MFCD00005127
• SMILES: CC(=C)C1CCC2(C(C1)O2)C

Upstream Synthesis Route

Limonene oxide, also known as limonene epoxide, is a cyclic ether compound that is derived from limonene, a naturally occurring terpene found in citrus fruits. In chemical synthesis, limonene oxide serves as a versatile building block that finds wide application in various reactions and transformations due to its unique structural properties.One important application of limonene oxide is as a chiral auxiliary in asymmetric synthesis. Its chiral nature allows it to influence the stereochemistry of reactions and facilitate the formation of enantiomerically pure compounds. By incorporating limonene oxide into a reaction, chemists can control the stereochemical outcome, leading to the selective formation of desired chiral products.Additionally, limonene oxide can undergo ring-opening reactions to produce functionalized derivatives that serve as key intermediates in the synthesis of complex organic molecules. The epoxide ring in limonene oxide is a reactive site that can be selectively opened under mild conditions, allowing access to a variety of functional groups for further elaboration.Furthermore, limonene oxide is utilized in the synthesis of various natural products, pharmaceuticals, and fine chemicals. Its compatibility with a range of reagents and catalysts enables chemists to perform diverse transformations, such as epoxidation, ring-opening reactions, and stereoselective functionalization, to access structurally complex molecules efficiently.Overall, the unique properties and reactivity of limonene oxide make it a valuable tool in chemical synthesis, enabling the construction of diverse molecular architectures with high selectivity and efficiency.