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  • 668192 - (S)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a;3,4- a′]dinaphthalen-4-yl)dimethylamine

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668192 Sigma-Aldrich

(S)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a;3,4- a′]dinaphthalen-4-yl)dimethylamine

97%

Synonym: (S)-MonoPhos®

  • CAS Number 185449-80-3

  • Empirical Formula (Hill Notation) C22H18NO2P

  • Molecular Weight 359.36

  •  MDL number MFCD03426988

  •  PubChem Substance ID 24884967

  •  NACRES NA.22

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, DSM MonoPhos Phosphoramidites, Privileged Ligands and Complexes More...
InChI Key   QCHAVHXSBZARBO-UHFFFAOYSA-N
assay   97%
mp   190 °C (dec.)

Description

Application

DSM MonoPhos Family of Highly Efficient Privileged Ligands

Packaging

1, 5 g in glass bottle

250 mg in glass insert

Legal Information

Sold under license from DSM for research purposes only.

MonoPhos is a registered trademark of DSM IP Assets B.V.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

DSM MonoPhos™

In collaboration with DSM, we are pleased to offer a range of MonoPhos™ ligands for the research market.† Feringa and co-workers have invented a diverse array of these chiral, monodentate phosphorami...
ChemFiles 2006, 6.8, 7.
Keywords: Addition reactions, Alkylations, Aminations, Annulations, Asymmetric synthesis, Building blocks, Catalysis, Cyclizations, Desymmetrizations, Drug discovery, Hydrogenations, Infrared spectroscopy, Ligands, Organic synthesis, Oxidations, Substitutions

Related Content

DSM MonoPhos Family- Highly Efficient Privileged Ligands

In collaboration with DSM, we are pleased to offer a range of MonoPhos™ ligands to the research market.† Feringa and co-workers have invented a diverse array of these chiral, monodentate phosphoramid...
Keywords: Addition reactions, Alkylations, Aminations, Annulations, Asymmetric synthesis, Building blocks, Catalysis, Cyclizations, Desymmetrizations, Drug discovery, Hydrogenations, Infrared spectroscopy, Ligands, Organic synthesis, Oxidations, Substitutions

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