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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)-

2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane

O=C1NCC2(C(=O)C1)CN(C2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane
CAS Number: 1105664-04-7
Product Number: AG0094O0(AGN-PC-0WA670)
Synonyms:
MDL No:
Molecular Formula: C12H18N2O4
Molecular Weight: 254.2823

Identification/Properties

Computed Properties
Molecular Weight:
254.286g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
254.127g/mol
Monoisotopic Mass:
254.127g/mol
Topological Polar Surface Area:
75.7A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
405
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 7,9-dioxo-2,6-diazaspiro[3.5]nonane-2-carboxylate is a versatile compound commonly employed in chemical synthesis. Its unique structure, featuring a spiro backbone with a tert-butyl and carboxylate moiety, enables it to participate in various synthetic pathways. One of its key applications lies in the field of medicinal chemistry, where it serves as a valuable building block for the synthesis of biologically active molecules. This compound's distinctive spiro structure imparts specific stereochemical features to the resulting products, making it particularly useful in asymmetric synthesis routes. Additionally, the presence of the tert-butyl group offers steric protection and can influence reactivity in certain reactions. Chemists utilize tert-Butyl 7,9-dioxo-2,6-diazaspiro[3.5]nonane-2-carboxylate as a strategic tool in designing and constructing complex molecular architectures with precise control over stereochemistry and functionality.