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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)-

1-[(3S)-3-PYRROLIDINYL]-PIPERIDINE DIHYDROCHLORIDE

C1CCN(CC1)[C@@H]1CNCC1.Cl.Cl Request for Quotation
Chemical Name: 1-[(3S)-3-PYRROLIDINYL]-PIPERIDINE DIHYDROCHLORIDE
CAS Number: 917505-12-5
Product Number: AG00IGV4(AGN-PC-0WA46S)
Synonyms:
MDL No:
Molecular Formula: C9H20Cl2N2
Molecular Weight: 227.1745

Identification/Properties

Computed Properties
Molecular Weight:
227.173g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
226.1g/mol
Monoisotopic Mass:
226.1g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
119
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


The (S)-1-(Pyrrolidin-3-yl)piperidine dihydrochloride, also known as $name$, is a versatile compound widely utilized in chemical synthesis processes. This compound plays a crucial role in asymmetric synthesis due to its chiral nature attributed to the (S) configuration. In organic chemistry, (S)-1-(Pyrrolidin-3-yl)piperidine dihydrochloride is commonly employed as a chiral auxiliary to induce stereochemical control in reactions.When used in chemical synthesis, (S)-1-(Pyrrolidin-3-yl)piperidine dihydrochloride facilitates the production of enantiomerically pure compounds. It serves as a valuable tool for chemists to access specific chiral molecules essential in pharmaceuticals, agrochemicals, and other fine chemicals. By harnessing the stereochemical properties of this compound, chemists can selectively synthesize desired enantiomers with high efficiency and precision.