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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

tert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate

O=C(N1CCC2(CC1)CCOC2=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate
CAS Number: 154348-08-0
Product Number: AG00AM4O(AGN-PC-0MXAY2)
Synonyms:
MDL No:
Molecular Formula: C13H21NO4
Molecular Weight: 255.3101

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate is a versatile compound that finds essential applications in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals and agrochemicals due to its unique structural properties. The presence of the tert-butyl group enhances the compound's stability and reactivity, making it a valuable intermediate in organic synthesis processes. Specifically, tert-Butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate can be utilized in the construction of intricate molecular structures, facilitating the formation of complex organic molecules with specific biological activities. Its spirocyclic structure imparts distinct stereochemical features that are crucial in the design and development of novel compounds with targeted properties. Furthermore, the presence of the carboxylate moiety allows for further derivatization, enabling the modification of the compound for a wide range of applications in medicinal chemistry and material science.