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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 2-benzyl-3-oxo-2,7-diazaspiro[3.5]nonane-7-carboxylate

O=C(N1CCC2(CC1)CN(C2=O)Cc1ccccc1)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 2-benzyl-3-oxo-2,7-diazaspiro[3.5]nonane-7-carboxylate
CAS Number: 155600-89-8
Product Number: AG001O14(AGN-PC-0MXRXZ)
Synonyms:
MDL No:
Molecular Formula: C19H26N2O3
Molecular Weight: 330.4213

Identification/Properties

Computed Properties
Molecular Weight:
330.428g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
330.194g/mol
Monoisotopic Mass:
330.194g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
483
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


As a chemist, I can explain the application of tert-Butyl 2-benzyl-1-oxo-2,7-diazaspiro[3.5]nonane-7-carboxylate in chemical synthesis. This compound is a versatile building block commonly used in organic chemistry for the synthesis of various biologically active molecules and pharmaceutical intermediates.Tert-Butyl 2-benzyl-1-oxo-2,7-diazaspiro[3.5]nonane-7-carboxylate possesses a unique spirocyclic structure which provides a rigid framework for introducing functional groups and stereochemical control during chemical reactions. The tert-butyl and benzyl groups can serve as protecting groups for sensitive functional moieties, allowing selective manipulations in the synthesis pathway.This compound can participate in a wide range of reactions such as acylation, alkylation, and reduction to generate diverse chemical entities. Its spirocyclic nature imparts conformational constraints that can influence the reactivity and selectivity of subsequent transformations, enabling the construction of complex molecular architectures efficiently.In summary, tert-Butyl 2-benzyl-1-oxo-2,7-diazaspiro[3.5]nonane-7-carboxylate plays a crucial role in chemical synthesis by serving as a key building block for the construction of structurally diverse and pharmacologically important compounds.