177-11-7 | 1,4-Dioxa-8-azaspiro[4.5]decane

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$12.00	$8.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$26.00	$18.00
100g	98%	in stock	$83.00	$58.00

Description

• Catalog Number: AA99689
• Chemical Name: 1,4-Dioxa-8-azaspiro[4.5]decane
• CAS Number: 177-11-7
• Molecular Formula: C7H13NO2
• Molecular Weight: 143.1836
• MDL Number: MFCD00005976
• SMILES: N1CCC2(CC1)OCCO2

Computed Properties

• Complexity: 113
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: -0.3

Upstream Synthesis Route

1,4-Dioxa-8-azaspiro[4.5]decane is a versatile compound that finds application in various chemical synthesis processes. It serves as a valuable building block for the development of novel organic compounds due to its unique spirocyclic structure. Specifically, in chemical synthesis, 1,4-Dioxa-8-azaspiro[4.5]decane plays a crucial role as a bridging molecule in the construction of complex molecular architectures.This compound is often utilized as a key intermediate in the synthesis of biologically active molecules, pharmaceuticals, and advanced materials. Its spirocyclic framework imparts stability and rigidity to the resulting molecules, thereby influencing their properties and potential applications. Additionally, the presence of heteroatoms in 1,4-Dioxa-8-azaspiro[4.5]decane enhances the diversity of chemical reactions it can participate in, leading to the formation of structurally intricate compounds.Furthermore, the incorporation of 1,4-Dioxa-8-azaspiro[4.5]decane in chemical synthesis strategies enables chemists to access new chemical space and design compounds with tailored functionalities. By leveraging the unique structural features of this compound, researchers can explore innovative synthetic pathways and discover novel materials with desired characteristics. In essence, 1,4-Dioxa-8-azaspiro[4.5]decane serves as a valuable tool in the hands of synthetic chemists, facilitating the creation of intricate molecular structures and expanding the frontiers of chemical science.

Literature

• Phosphorus-nitrogen compounds. Part 23: syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclotriphosphazenes.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120201

• Phosphorus-nitrogen compounds. Part 20: Fully substituted spiro-cyclotriphosphazenic lariat (PNP-pivot) ether derivatives.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100801

• Phosphorus-nitrogen compounds. Part 13. Syntheses, crystal structures, spectroscopic, stereogenic, and anisochronic properties of novel spiro-ansa-spiro-, spiro-bino-spiro-, and spiro-crypta phosphazene derivatives.

  Inorganic chemistry 20061016

• Ruthenium-catalyzed anti-Markovnikov hydroamination of vinylarenes.

  Journal of the American Chemical Society 20040310