10276-21-8 | Isophorone oxide

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$19.00	$13.00
25g	95%	in stock	$26.00	$18.00
100g	95%	in stock	$60.00	$42.00
500g	95%	in stock	$289.00	$202.00

Description

• Catalog Number: AA10572
• Chemical Name: Isophorone oxide
• CAS Number: 10276-21-8
• Molecular Formula: C9H14O2
• Molecular Weight: 154.20626000000001
• MDL Number: MFCD00085465
• SMILES: O=C1CC(C)(C)CC2(C1O2)C
• NSC Number: 63367

Computed Properties

• Complexity: 220
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Undefined Atom Stereocenter Count: 2
• XLogP3: 1.2

Upstream Synthesis Route

4,4,6-Trimethyl-7-oxabicyclo[4.1.0]heptan-2-one, also known as $name$, is a versatile compound commonly utilized in chemical synthesis processes. This unique molecule plays a crucial role as a building block for the creation of various pharmaceuticals, agrochemicals, fragrances, and other specialty chemicals. Its compact and rigid structure, with a bicyclic framework incorporating oxygen heteroatoms, enables it to serve as a valuable intermediate in the production of complex organic molecules.In chemical synthesis, $name$ can be employed as a precursor for the synthesis of biologically active compounds due to its ability to undergo diverse transformations. Its structural features make it a valuable starting material for the construction of intricate molecular frameworks, allowing chemists to access a wide range of structural motifs efficiently. Additionally, the presence of the ketone moiety in $name$ enables functional group manipulation, further expanding its synthetic utility.Furthermore, the stereochemistry and reactivity of 4,4,6-Trimethyl-7-oxabicyclo[4.1.0]heptan-2-one make it an attractive candidate for chiral synthesis applications. By utilizing this compound as a chiral building block, chemists can access enantiomerically pure compounds with high stereochemical control, paving the way for the production of optically active molecules with enhanced biological activities or selective properties.Overall, the strategic incorporation of $name$ into chemical synthesis workflows allows for the efficient construction of complex molecules with diverse functionalities, making it an indispensable tool for synthetic chemists seeking to access structurally diverse compounds for various applications.