Atomfair 2,5-Dioxaspiro[3.5]nonan-8-amine C7H13NO2

Description 2,5-Dioxaspiro[3.5]nonan-8-amine (CAS No. 1934361-63-3) is a high-purity spirocyclic amine compound with the molecular formula C7H13NO2. This specialized heterocyclic amine features a unique spiro[3.5]nonane core structure with two oxygen atoms incorporated into the ring system, making it a valuable building block for pharmaceutical and materials science research. The compound is supplied as a stable solid with rigorous quality control to ensure batch-to-batch consistency. Its structural complexity offers diverse functionalization possibilities for medicinal chemistry applications, particularly in the development of novel bioactive molecules. Suitable for use in organic synthesis, catalyst development, and as a precursor for advanced materials.

Description

2,5-Dioxaspiro[3.5]nonan-8-amine (CAS No. 1934361-63-3) is a high-purity spirocyclic amine compound with the molecular formula C₇H₁₃NO₂. This specialized heterocyclic amine features a unique spiro[3.5]nonane core structure with two oxygen atoms incorporated into the ring system, making it a valuable building block for pharmaceutical and materials science research. The compound is supplied as a stable solid with rigorous quality control to ensure batch-to-batch consistency. Its structural complexity offers diverse functionalization possibilities for medicinal chemistry applications, particularly in the development of novel bioactive molecules. Suitable for use in organic synthesis, catalyst development, and as a precursor for advanced materials.

CAS No: 1934361-63-3
Molecular Formula: C7H13NO2
Molecular Weight: 143.18
Exact Mass: 143.094628657
Monoisotopic Mass: 143.094628657
IUPAC Name: 2,5-dioxaspiro[3.5]nonan-8-amine
SMILES: C1COC2(CC1N)COC2
Synonyms: 2,5-Dioxaspiro[3.5]nonan-8-amine, 1934361-63-3

Application

2,5-Dioxaspiro[3.5]nonan-8-amine serves as a versatile intermediate in organic synthesis, particularly for constructing complex spirocyclic frameworks found in bioactive compounds. Researchers utilize this amine in pharmaceutical development for creating novel drug candidates with potential CNS activity. The spirocyclic structure makes it valuable for developing conformationally constrained analogs in medicinal chemistry programs. Additionally, it finds application in materials science as a building block for specialty polymers and advanced functional materials.

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