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Home  > 2-Oxa-6-azaspiro[3.3]heptane hemioxalate

AB44202

1045709-32-7 | 2-Oxa-6-azaspiro[3.3]heptane hemioxalate

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $11.00 $8.00 -   +
5g 98% in stock $23.00 $17.00 -   +
10g 98% in stock $41.00 $29.00 -   +
15g 98% in stock $61.00 $43.00 -   +
25g 98% in stock $100.00 $70.00 -   +
100g 98% in stock $394.00 $276.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB44202
Chemical Name: 2-Oxa-6-azaspiro[3.3]heptane hemioxalate
CAS Number: 1045709-32-7
Molecular Formula: C12H20N2O6
Molecular Weight: 288.297
MDL Number: MFCD16652332
SMILES: N1CC2(C1)COC2.N1CC2(C1)COC2.OC(=O)C(=O)O

 

Computed Properties
Complexity: 154  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 2-Oxa-6-azaspiro[3.3]heptane oxalate(2:1)is a versatile compound that finds wide application in chemical synthesis, particularly in the field of heterocyclic chemistry. As a fused bicycle compound, it offers unique structural features that make it valuable for creating complex molecules with diverse functionalities.In chemical synthesis, 2-Oxa-6-azaspiro[3.3]heptane oxalate (2:1) serves as a key building block for the construction of novel heterocyclic compounds. Its spirocyclic structure provides a rigid framework that can impart specific stereochemical properties to the synthesized molecules, making it ideal for designing chiral ligands, pharmaceuticals, and bioactive compounds.Furthermore, the presence of oxalate groups in the compound offers opportunities for further functionalization through reactions such as transesterification, esterification, and cross-coupling reactions. This allows for the introduction of additional substituents or functional groups, enhancing the diversity and complexity of the synthesized molecules.Overall, the use of 2-Oxa-6-azaspiro[3.3]heptane oxalate (2:1) in chemical synthesis enables the efficient and strategic construction of diverse heterocyclic compounds with potential applications in medicinal chemistry, materials science, and agrochemical research.
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