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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)-

Piperidine, 1-(3-azetidinyl)-, hydrochloride (1:2)

C1CCN(CC1)C1CNC1.Cl.Cl Request for Quotation
Chemical Name: Piperidine, 1-(3-azetidinyl)-, hydrochloride (1:2)
CAS Number: 178312-57-7
Product Number: AG0025X4(AGN-PC-0WB6MP)
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:
1
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:
104
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Piperidin-1-yl)azetidine dihydrochloride is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and biologically active molecules. Its unique chemical structure allows for efficient incorporation into complex molecular frameworks, making it an essential reagent in organic synthesis. The presence of the piperidine and azetidine moieties imparts favorable properties to the molecule, enabling it to participate in key chemical reactions such as ring-closing, nucleophilic substitution, and cross-coupling reactions. Furthermore, the dihydrochloride salt form enhances the compound's solubility and stability, facilitating its use in a wide range of synthesis processes. Overall, 3-(Piperidin-1-yl)azetidine dihydrochloride serves as a valuable tool for chemists in the development of novel compounds with diverse applications.