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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-oxa-6-azaspiro[3.3]heptane-6-carboxylate

O=C(N1CC2(C1)COC2)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 2-oxa-6-azaspiro[3.3]heptane-6-carboxylate
CAS Number: 1263285-88-6
Product Number: AG009XDZ(AGN-PC-080U00)
Synonyms:
MDL No:
Molecular Formula: C10H17NO3
Molecular Weight: 199.2469

Identification/Properties

Computed Properties
Molecular Weight:
199.25g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
199.121g/mol
Monoisotopic Mass:
199.121g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
245
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 2-oxa-6-azaspiro[3.3]heptane-6-carboxylate compound is a versatile building block in chemical synthesis, offering a wide range of applications in organic chemistry. Its unique structure and reactivity make it valuable for various transformations in the laboratory setting.In chemical synthesis, tert-Butyl 2-oxa-6-azaspiro[3.3]heptane-6-carboxylate can serve as a key intermediate for the preparation of complex molecules and heterocyclic compounds. Its spirocyclic motif provides a scaffold for further functionalization and derivatization, allowing chemists to fine-tune the properties of the final products.This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other bioactive compounds due to its ability to introduce structural diversity and stereochemical complexity into molecules. Its presence can impart desired biological activities or pharmacokinetic properties to the target molecules.Additionally, tert-Butyl 2-oxa-6-azaspiro[3.3]heptane-6-carboxylate can participate in various types of reactions such as nucleophilic substitutions, ring-opening reactions, and cycloadditions, enabling chemists to access a wide variety of chemical structures efficiently.Overall, the application of tert-Butyl 2-oxa-6-azaspiro[3.3]heptane-6-carboxylate in chemical synthesis offers chemists a powerful tool for designing and synthesizing complex molecules with diverse functionalities and potential biological activities.