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CAS 1031927-14-6

:

1,9-Diazaspiro[5.5]undecane-9-carboxylic acid,1,1-dimethylethyl ester

Description:
1,9-Diazaspiro[5.5]undecane-9-carboxylic acid, 1,1-dimethylethyl ester, identified by its CAS number 1031927-14-6, is a chemical compound characterized by its unique spirocyclic structure, which incorporates two nitrogen atoms within a bicyclic framework. This compound features a carboxylic acid functional group that is esterified with a tert-butyl group, contributing to its lipophilicity and potential applications in organic synthesis and medicinal chemistry. The presence of the diaza moiety suggests potential biological activity, as nitrogen-containing compounds often exhibit diverse pharmacological properties. Additionally, the spiro structure can influence the compound's conformational flexibility and steric interactions, which are critical in drug design. Its synthesis and reactivity may be of interest in the development of novel therapeutic agents or as intermediates in chemical reactions. Overall, this compound exemplifies the complexity and versatility of nitrogen-containing heterocycles in organic chemistry.
Formula:C14H26N2O2
Synonyms:
  • 1,9-Diazaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester
  • tert-Butyl 1,9-diazaspiro[5.5]undecane-9-carboxylate, 9-(tert-Butoxycarbonyl)-1,9-diazaspiro[5.5]undecane
  • 1,9-Diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester - D6007
  • 9-Boc-1,9-diazaspiro[5.5]undecane
  • 1,9-Diazaspiro[5.5]undecane-9-carboxylic acid tert-butyl ester
  • 1,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester
  • 1,9-Diazaspiro[5.5]undecane-9-carboxylic acid
  • 1,9-Diazaspiro[5.5]undecane-9-carboxylic acid, 1,1-dimethylethyl ester
  • 1,9-Diazaspiro[5.5]undecane, N9-BOC protected 95+%
  • 1,9-Diazaspiro[5.5]undecane, N9-BOC protected
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