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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 4-oxo-1-azaspiro[4.4]nonane-1-carboxylate

O=C(N1CCC(=O)C21CCCC2)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-oxo-1-azaspiro[4.4]nonane-1-carboxylate
CAS Number: 1540034-11-4
Product Number: AG01AUFL(AG01AUFL)
Synonyms:
MDL No:
Molecular Formula: C13H21NO3
Molecular Weight: 239.3107

Identification/Properties

Computed Properties
Molecular Weight:
239.315g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
239.152g/mol
Monoisotopic Mass:
239.152g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
337
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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 4-oxo-1-azaspiro[4.4]nonane-1-carboxylate is a versatile compound used in chemical synthesis for the creation of a diverse range of molecules. In organic chemistry, this compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactive properties allow for the formation of complex structures and the modification of functional groups in a controlled manner. By incorporating tert-Butyl 4-oxo-1-azaspiro[4.4]nonane-1-carboxylate into synthetic pathways, chemists can achieve efficient and selective transformations, enabling the development of new molecules with desired properties and applications.