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  2. 7-Oxo-2,6-diazaspiro[3.4]octane-2-carboxylic acid tert-butyl ester

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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)-

7-Oxo-2,6-diazaspiro[3.4]octane-2-carboxylic acid tert-butyl ester

O=C1NCC2(C1)CN(C2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 7-Oxo-2,6-diazaspiro[3.4]octane-2-carboxylic acid tert-butyl ester
CAS Number: 1234616-51-3
Product Number: AG000KNC(AGN-PC-0WAC9M)
Synonyms:
MDL No:
Molecular Formula: C11H18N2O3
Molecular Weight: 226.2722

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
226.276g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
226.132g/mol
Monoisotopic Mass:
226.132g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
327
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 7-oxo-2,6-diazaspiro[3.4]octane-2-carboxylate is a versatile compound that finds extensive application in chemical synthesis. It serves as a valuable building block in the creation of novel organic molecules due to its unique structural features and reactivity. In the realm of organic synthesis, this compound acts as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials. Its spirocyclic framework offers a strategic advantage in designing complex molecular structures, enabling chemists to efficiently construct diverse chemical entities. Furthermore, the presence of the tert-butyl and carboxylate groups provides opportunities for further functionalization, enhancing the compound's utility in the synthesis of specialized compounds with tailored properties.