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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-2,9-diazaspiro[4.5]decane-9-carboxylate

O=C(N1CCCC2(C1)CCNC2=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 1-oxo-2,9-diazaspiro[4.5]decane-9-carboxylate
CAS Number: 923009-50-1
Product Number: AG0036RJ(AGN-PC-07YK5Y)
Synonyms:
MDL No:
Molecular Formula: C13H22N2O3
Molecular Weight: 254.3254

Identification/Properties

Properties
BP:
425℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
254.33g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
254.163g/mol
Monoisotopic Mass:
254.163g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
362
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is a versatile compound widely utilized in chemical synthesis due to its unique structure and reactivity. This compound serves as a valuable building block in the creation of complex molecules and pharmaceutical intermediates. Its spirocyclic structure imparts interesting stereochemical properties that make it ideal for the synthesis of chiral compounds. Additionally, the tert-butyl ester group provides stability and facilitates easy purification during synthesis processes. Chemists often employ this compound in the development of new drug candidates, agrochemicals, and materials due to its synthetic flexibility and ability to introduce structural diversity.