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2-OXA-8-AZASPIRO[4.5]DECAN-1-ONE HYDROCHLORIDE is a white crystalline powder that is a member of the spiro compounds class. It is soluble in water and ethanol, and has potential pharmaceutical applications, making it a valuable building block in the synthesis of various organic compounds. However, it is crucial to handle this chemical with care due to its potential health hazards.

4427-25-2

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4427-25-2 Usage

Uses

Used in Pharmaceutical Industry:
2-OXA-8-AZASPIRO[4.5]DECAN-1-ONE HYDROCHLORIDE is used as a building block for the synthesis of various organic compounds, particularly in the development of new pharmaceuticals. Its unique structure and properties make it a promising candidate for creating innovative drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, 2-OXA-8-AZASPIRO[4.5]DECAN-1-ONE HYDROCHLORIDE is utilized as a key component in the exploration of new chemical reactions and synthesis pathways. Its versatility and reactivity contribute to the advancement of scientific knowledge and the discovery of novel applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 4427-25-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4427-25:
(6*4)+(5*4)+(4*2)+(3*7)+(2*2)+(1*5)=82
82 % 10 = 2
So 4427-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c10-7-8(3-6-11-7)1-4-9-5-2-8/h9H,1-6H2

4427-25-2Downstream Products

4427-25-2Relevant academic research and scientific papers

4,4-Disubstituted cyclohexylamine NK1 receptor antagonists II

Cooper, Laura C.,Carlson, Emma J.,Castro, Jose L.,Chicchi, Gary G.,Dinnell, Kevin,Di Salvo, Jerry,Elliott, Jason M.,Hollingworth, Gregory J.,Kurtz, Marc M.,Ridgill, Mark P.,Rycroft, Wayne,Tsao, Kwei-Lan,Swain, Christopher J.

, p. 1759 - 1762 (2007/10/03)

A series of novel 4,4-disubstituted cyclohexylamines as NK1 receptor antagonists is described: modifications to the amine moiety retain NK1 receptor binding affinity whilst disrupting IKr affinity.

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