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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-methyl-2,7-diazaspiro[3.5]nonane;dihydrochloride

CN1CC2(C1)CCNCC2.Cl.Cl Request for Quotation
Chemical Name: 2-methyl-2,7-diazaspiro[3.5]nonane;dihydrochloride
CAS Number: 1610028-42-6
Product Number: AG00AO7Y(AGN-PC-0JK1JQ)
Synonyms:
MDL No:
Molecular Formula: C8H18Cl2N2
Molecular Weight: 213.1479

Identification/Properties

Computed Properties
Molecular Weight:
213.146g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
212.085g/mol
Monoisotopic Mass:
212.085g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
119
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-2,7-diazaspiro[3.5]nonane dihydrochloride is a versatile compound widely utilized in chemical synthesis for its unique properties and applications. This compound serves as a valuable building block in the creation of various complex organic molecules and pharmaceutical agents. Its spirocyclic structure offers a rigid framework that can impart conformational constraints and enhance the stereochemical outcomes of synthetic reactions. In particular, 2-Methyl-2,7-diazaspiro[3.5]nonane dihydrochloride is commonly employed in the synthesis of drug candidates and biologically active compounds due to its ability to influence molecular shape and reactivity. Additionally, its presence in synthetic pathways often leads to improved selectivity and efficiency in the formation of desired products. In research and development settings, this compound plays a crucial role in expanding the chemical toolbox available to chemists for the construction of diverse molecular architectures with potential therapeutic or industrial significance.