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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)-

2,6-Diaza-spiro[3.5]nonane dihydrochloride

C1CCC2(CN1)CNC2.Cl.Cl Request for Quotation
Chemical Name: 2,6-Diaza-spiro[3.5]nonane dihydrochloride
CAS Number: 1334499-63-6
Product Number: AG003G1Y(AGN-PC-0WA5SD)
Synonyms:
MDL No:
Molecular Formula: C7H16Cl2N2
Molecular Weight: 199.1213

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
199.119g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
198.069g/mol
Monoisotopic Mass:
198.069g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
108
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:
3
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


2,6-Diazaspiro[3.5]nonane dihydrochloride serves as a valuable reagent in chemical synthesis due to its unique structural properties. This compound is commonly employed as a versatile building block in the creation of complex organic molecules and heterocyclic compounds. Its asymmetric nature allows for the generation of diverse chiral structures, making it particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the presence of the dihydrochloride group enhances the compound's solubility and stability, facilitating its manipulation in various synthetic reactions. By incorporating 2,6-Diazaspiro[3.5]nonane dihydrochloride into synthetic pathways, chemists can access novel molecular architectures with potential biological activities and material properties.