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(R)-MONOPHOS

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(R)-MONOPHOS Basic information

Product Name:
(R)-MONOPHOS
Synonyms:
  • (R)-(-)-[4-N,N-Dimethylamino]dinaphtho[2.1-d:1'.2'-f][1.3.2]dioxaphosphepine(R)-monophos]
  • (R)-(-)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a
  • 3,4-a']dinaphthalen-4-yl)dimethylamine,min.97%(R)-MONOPHOS
  • (R)-(-)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a:3,4-a']dinaphthalen-4-yl)dimethylamine, min. 97% (R)-MONOPHOS
  • 3,4-a']dinaphthalen-4-yl)dimethylamine
  • (R)-()-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a:3,4-a′]di-naphthalen-4-yl)dimethylamine,(R)-Monophos
  • 3,4-a']dinaphthalen
  • 3,4-a']dinaphthalen-4-yl)[(1S)-1-phenylethyl]-aMine
CAS:
157488-65-8
MF:
C22H18NO2P
MW:
359.36
Product Categories:
  • SF160006
  • Chiral Phosphine
  • CPN
Mol File:
157488-65-8.mol
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(R)-MONOPHOS Chemical Properties

Melting point:
190 °C (dec.)
alpha 
-583° (c 0.06, CHCl3)
Boiling point:
548.7±33.0 °C(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
crystal
pka
1.22±0.20(Predicted)
color 
white
Sensitive 
air sensitive
InChIKey
QCHAVHXSBZARBO-UHFFFAOYSA-N
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
TSCA 
No
HS Code 
2934.99.4400

MSDS

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(R)-MONOPHOS Usage And Synthesis

Reaction

  1. Ligand used in the enantioselective, rhodium-catalyzed hydrogenation of substituted olefins, such as N-acetyldihydroamino acids, enamides, and unsaturated acids.
  2. Ligand used in the enantioselective, iridium-catalyzed allylic substitution of allyl acetates containing only a single substituent in the 1 or 3 position.
  3. Ligand use in the rhodium-catalyzed, amide directed, asymmetric hydroboration reaction.
  4. Ligand used in asymmetric conjugate addition of aryl boronic acids to dihydronitronaphthalenes.
  5. Ligand used in the rhodium-catalyzed asymmetric intramolecular 1,4 addition.

Uses

DSM MonoPhos Family of Highly Efficient Privileged Ligands

(R)-MONOPHOSSupplier

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