| Identification | Back Directory | [Name]
1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER | [CAS]
939793-21-2 | [Synonyms]
1,7-Diaza-spiro[4.5]decan...
tert-butyl 1,7-diazaspiro[4.5]decane-7-carboxylate
tert-butyl 1,9-diazaspiro[4.5]decane-9-carboxylate
1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER
1,7-Diazaspiro[4.5]decane-7-carboxylic acid, 1,1-dimethylethyl ester
1,7-Diazaspiro[4.5]decane-7-carboxylic acid tert-butyl ester - D5999 | [Molecular Formula]
C13H24N2O2 | [MDL Number]
MFCD08752633 | [MOL File]
939793-21-2.mol | [Molecular Weight]
240.34 |
| Chemical Properties | Back Directory | [storage temp. ]
2-8°C(protect from light) | [Appearance]
Colorless to light yellow Liquid | [InChI]
InChI=1S/C13H24N2O2/c1-12(2,3)17-11(16)15-9-5-7-13(10-15)6-4-8-14-13/h14H,4-10H2,1-3H3 | [InChIKey]
PDFULYHFVRJQJO-UHFFFAOYSA-N | [SMILES]
N1C2(CCCN(C(OC(C)(C)C)=O)C2)CCC1 |
| Hazard Information | Back Directory | [Uses]
tert-Butyl-1,7-diazaspiro[4.5]decane-7-carboxylate is a useful reagent in preparation of spiro heterocycles as phosphodiesterase inhibitors. | [Pharmaceutical Applications]
The major structure of 1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER, Spiro[4.5]decane, functions as a key intermediate in organic synthesis, particularly for the preparation of pharmaceutical derivatives. For instance, it has been employed in the synthesis of spiro[4.5]decane-based analogues of 1α,25-dihydroxyvitamin D3, which exhibit potential biological activity relevant to therapeutic applications.[1] | [References]
[1] Synthesis of Spiro[4.5]decane CF-Ring Analogues of 1α,25-Dihydroxyvitamin D3. Org. Lett. 2006, 8, 19, 4247–4250. DOI:10.1021/ol061575p
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