CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
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  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane
  • CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane

CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane

CAS NO:937729-06-1 NAME:8-Boc-1,8-diazaspiro[4.5]decane MF:C13H24N2O2 MW:240.34 Purity:98% COA:Provide Sample:Negotiable Appearance:White to light yellow (Solid)

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Material Chemistry

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Product introduction

PRODUCT NAME  8-Boc-1,8-diazaspiro[4.5]decane
CAS NO 937729-06-1
Synonyms tert-butyl 1,8-diazaspiro[4.5]decane-8-carboxylate
1,8-Diazaspiro[4.5]decane-8-carboxylic acid tert-butyl ester
BP 337.0±35.0 °C(Predicted)
DENSITY 1.07±0.1 g/cm3(Predicted)
STORAGE 2-8°C
DELIVERY 2-3DAYS
PACKAGE According client's request

Description of CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane

The tert-butyl 1,8-diazaspiro[4.5]decane-8-carboxylate CAS NO:937729-06-1  is a compound that belongs to the class of spirocyclic compounds, which are characterized by their unique structures where two rings are joined at a single atom. The compound mentioned is not directly studied in the provided papers, but related compounds with similar spirocyclic frameworks have been synthesized and analyzed, providing insights into the chemical behavior and properties of such structures.
 

 

 


Applications of CAS NO:937729-06-1 8-Boc-1,8-diazaspiro[4.5]decane

1)Supramolecular Arrangements
Spirohydantoin derivatives, including Tert-butyl 1,8-diazaspiro[4.5]decane-8-carboxylate variants
2)Conformational Analysis
3)Mirror Symmetry and Molecular Structure
4)Stereoselective Synthesis
They have been used in stereoselective synthesis, demonstrating their utility in creating specific molecular configurations for advanced chemical applications

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