104-50-7 | Gamma-octanoic lactone

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$8.00	$5.00
25g	95%	in stock	$10.00	$7.00
100g	95%	in stock	$36.00	$25.00
250g	95%	in stock	$69.00	$48.00
500g	95%	in stock	$136.00	$95.00
1kg	95%	in stock	$148.00	$103.00
5kg	95%	in stock	$569.00	$398.00
10kg	95%	in stock	$855.00	$598.00

Description

• Catalog Number: AB74420
• Chemical Name: Gamma-octanoic lactone
• CAS Number: 104-50-7
• Molecular Formula: C8H14O2
• Molecular Weight: 142.19555999999997
• MDL Number: MFCD00005402
• SMILES: CCCCC1CCC(=O)O1

Computed Properties

• Complexity: 120
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

5-Butyldihydrofuran-2(3H)-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structure and reactivity. In chemical synthesis, $name$ is commonly employed as a starting material for the preparation of functionalized derivatives through a series of synthetic transformations.One key application of $name$ in chemical synthesis is its use in the formation of heterocyclic compounds. By incorporating $name$ into reaction schemes, chemists can access a diverse array of heterocycles with different ring sizes and substitution patterns. This enables the creation of complex molecular structures with specific pharmacological, biological, or material properties.Furthermore, $name$ can also participate in various types of chemical reactions, such as oxidation, reduction, and functional group interconversion. Its ability to undergo these transformations makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.Overall, the role of 5-Butyldihydrofuran-2(3H)-one in chemical synthesis is pivotal for the construction of diverse organic compounds with strategic functionalization and structural diversity. Its versatility and reactivity make it a fundamental component in the toolkit of synthetic chemists seeking to access novel molecules for various applications.