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Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate

Catalog Number
ACM1092934194
Product Name
Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate
CAS
1092934-19-4
  • Product Overview
  • Usage
Synonyms
Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate;(R)-BINSA Dipotassium Salt;1092934-19-4;SCHEMBL3628026;MFCD28386102;D4445;(R)-1,1'-Binaphthyl-2,2'-disulfonic Acid Dipotassium Salt;
IUPAC Name
dipotassium;1-(2-sulfonatonaphthalen-1-yl)naphthalene-2-sulfonate;
Molecular Weight
490.627g/mol
Molecular Formula
C20H12K2O6S2;
Canonical SMILES
C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)S(=O)(=O)[O-])S(=O)(=O)[O-].[K+].[K+];
InChI
InChI=1S/C20H14O6S2.2K/c21-27(22,23)17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)28(24,25)26;;/h1-12H,(H,21,22,23)(H,24,25,26);;/q;2*+1/p-2;
InChI Key
ALWKFXOUXLSOSQ-UHFFFAOYSA-L;
Complexity
673
Covalently-Bonded Unit Count
3
Exact Mass
489.935g/mol
H-Bond Acceptor
6
Heavy Atom Count
30
Monoisotopic Mass
489.935g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
131A^2
Application
Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate serves as a vital catalyst in asymmetric Mannich reactions. These reactions are essential in the synthesis of various compounds, as the catalyst facilitates the formation of carbon-nitrogen bonds with high selectivity, promoting the production of enantiomerically pure substances. This particular catalyst's efficiency and selectivity make it an invaluable tool for researchers and chemists working on synthesizing complex organic molecules.
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