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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)-

6-Azoniaspiro[5.5]undecane, chloride

C1CC[N+]2(CC1)CCCCC2.[Cl-] Request for Quotation
Chemical Name: 6-Azoniaspiro[5.5]undecane, chloride
CAS Number: 56496-16-3
Product Number: AG00EFZU(AGN-PC-0KKTKN)
Synonyms:
MDL No:
Molecular Formula: C10H20ClN
Molecular Weight: 189.7255

Identification/Properties

Computed Properties
Molecular Weight:
189.727g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
189.128g/mol
Monoisotopic Mass:
189.128g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
99.3
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-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Azaspiro[5.5]undecan-6-ium chloride is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the creation of diverse heterocyclic structures. Its spirocyclic framework allows for the synthesis of complex molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 6-Azaspiro[5.5]undecan-6-ium chloride can act as a key intermediate in the formation of various nitrogen-containing compounds. Its presence in a reaction scheme can facilitate the introduction of an azaspiro moiety into target molecules, providing them with enhanced biological activity or other desired properties. The positively charged nature of the chloride salt enhances its reactivity, making it a valuable reagent for forging new carbon-nitrogen bonds in a controlled manner.Furthermore, this compound's spirocyclic structure imparts rigidity and three-dimensionality to the molecules it is incorporated into, potentially influencing their interactions with biological targets or catalytic sites. By judiciously incorporating 6-Azaspiro[5.5]undecan-6-ium chloride into synthetic pathways, chemists can access a diverse array of compounds with tailored structures and functions for various applications in the field of chemistry.