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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-OIAZASPIRO945)DECANE

N1CCC2(CC1)CNCC2 Request for Quotation
Chemical Name: 2,8-OIAZASPIRO945)DECANE
CAS Number: 176-67-0
Product Number: AG0021D3(AGN-PC-0WA5U5)
Synonyms:
MDL No:
Molecular Formula: C8H16N2
Molecular Weight: 140.2260

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
140.23g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
140.131g/mol
Monoisotopic Mass:
140.131g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
116
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[4.5]decane is a valuable compound widely used in chemical synthesis as a versatile building block. Its unique structure, consisting of a spirocyclic framework with two nitrogen atoms, offers a range of opportunities for creating novel molecules with diverse functionalities.One key application of 2,8-Diazaspiro[4.5]decane is in the preparation of heterocyclic compounds. By incorporating this compound into chemical reactions, chemists can access a variety of complex ring systems that are essential in drug discovery and material science. The presence of nitrogen atoms in the spirocyclic core also enables the modification of its chemical properties, allowing for further derivatization and customization of the final products.Furthermore, 2,8-Diazaspiro[4.5]decane serves as a valuable chiral scaffold in asymmetric synthesis. Its chiral nature can be harnessed to induce chirality in neighboring functional groups, leading to the formation of enantioenriched compounds with high optical purity. This property is particularly important in the pharmaceutical industry, where enantiopure molecules are crucial for the development of safe and effective drugs.In summary, the application of 2,8-Diazaspiro[4.5]decane in chemical synthesis offers a wealth of opportunities for creating complex molecules, exploring new reaction pathways, and accessing enantioenriched compounds with potential applications in various fields of science and industry.