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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)-

(S)-1,3'-Bipyrrolidine dihydrochloride

C1NC[C@H](C1)N1CCCC1.Cl.Cl Request for Quotation
Chemical Name: (S)-1,3'-Bipyrrolidine dihydrochloride
CAS Number: 956605-97-3
Product Number: AG00ILCD(AGN-PC-0WAICI)
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:
108
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-1,3'-Bipyrrolidine dihydrochloride is a versatile and highly selective chiral catalyst that plays a crucial role in asymmetric synthesis. This compound is widely used in various chemical reactions to facilitate the formation of enantiomerically pure products. Specifically, (S)-1,3'-Bipyrrolidine dihydrochloride is employed as a catalyst in asymmetric cycloaddition reactions, such as Diels-Alder reactions, which are essential in the production of pharmaceuticals, agrochemicals, and natural product synthesis. Its ability to control the stereochemistry of the products makes it a valuable tool for chemists working in the field of organic synthesis. Additionally, its compatibility with a wide range of substrates and reaction conditions further enhances its utility in the development of efficient and selective synthetic methodologies.