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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 2,6-diazaspiro[3.3]heptane-2-carboxylate;oxalic acid

O=C(N1CC2(C1)CNC2)OC(C)(C)C.OC(=O)C(=O)O Request for Quotation
Chemical Name: tert-butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate;oxalic acid
CAS Number: 1227382-01-5
Product Number: AG000J8A(AGN-PC-09R4KD)
Synonyms:
MDL No:
Molecular Formula: C12H20N2O6
Molecular Weight: 288.2970

Identification/Properties

Computed Properties
Molecular Weight:
288.3g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
288.132g/mol
Monoisotopic Mass:
288.132g/mol
Topological Polar Surface Area:
116A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
317
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:
2
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 2,6-diazaspiro[3.3]heptane-2-carboxylate oxalate is a versatile compound in chemical synthesis, particularly valued for its role in asymmetric synthesis strategies. This compound serves as an important chiral building block, facilitating the creation of enantiomerically enriched compounds in organic chemistry. Its unique spirocyclic structure provides a valuable scaffold for constructing complex molecules with high stereoselectivity. By incorporating tert-Butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate oxalate into synthetic routes, chemists can access a diverse array of chiral compounds with potential applications in pharmaceuticals, agrochemicals, and materials science. The compound's ability to control the stereochemistry of reactions makes it a valuable tool for designing and synthesizing new molecules with tailored properties and functionalities.