1. Home
  2. (S)-3-(Piperidin-2-yl)pyridine dihydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

(S)-3-(Piperidin-2-yl)pyridine dihydrochloride

C1CC[C@H](NC1)c1cccnc1.Cl.Cl Request for Quotation
Chemical Name: (S)-3-(Piperidin-2-yl)pyridine dihydrochloride
CAS Number: 31945-06-9
Product Number: AG01D94I(AGN-PC-0WNGO1)
Synonyms:
MDL No:
Molecular Formula: C10H16Cl2N2
Molecular Weight: 235.1534

Identification/Properties

Computed Properties
Molecular Weight:
235.152g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
234.069g/mol
Monoisotopic Mass:
234.069g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
136
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

Request for Quotation

Customer Feedback

Chemical Structure


(S)-3-(Piperidin-2-yl)pyridine dihydrochloride is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique structure and chirality make it an essential component in the development of various pharmaceuticals, agrochemicals, and fine chemicals. The compound can serve as a key intermediate in the synthesis of complex organic molecules due to its ability to introduce chirality at specific positions in the target molecule. This compound's application in asymmetric synthesis allows researchers to efficiently access enantiomerically pure compounds, leading to improved drug efficacy and reduced side effects in pharmaceuticals. Additionally, (S)-3-(Piperidin-2-yl)pyridine dihydrochloride plays a crucial role in the creation of novel materials and catalysts with advanced functional properties, making it a valuable tool for modern chemical research and development.