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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)-

2,8-Diazaspiro[5.5]undecane

C1CCC2(CN1)CCCNC2 Request for Quotation
Chemical Name: 2,8-Diazaspiro[5.5]undecane
CAS Number: 180-50-7
Product Number: AG0021KM(AGN-PC-00Q0UQ)
Synonyms:
MDL No:
Molecular Formula: C9H18N2
Molecular Weight: 154.2526

Identification/Properties

Computed Properties
Molecular Weight:
154.257g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
154.147g/mol
Monoisotopic Mass:
154.147g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
118
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


2,8-Diazaspiro[5.5]undecane, also known as $name$, is a versatile compound widely used in chemical synthesis. This unique molecule contains two nitrogen atoms and a spiro ring system, making it valuable in various synthetic protocols. In chemical synthesis, $name$ serves as a building block for creating complex organic compounds due to its ability to introduce nitrogen functionalities into the target molecules. By utilizing the distinct structural features of $name$, chemists can access novel chemical pathways and design efficient routes to intricate organic structures. Additionally, the spiro ring framework of $name$ imparts steric and electronic properties that are crucial for controlling reactivity and selectivity in synthetic reactions. Overall, the application of 2,8-Diazaspiro[5.5]undecane in chemical synthesis offers a strategic approach for constructing diverse chemical scaffolds and advancing the development of new materials and pharmaceuticals.