| Identification | Back Directory | [Name]
Chlorobis(cyclooctene)rhodium(I) dimer | [CAS]
12279-09-3 | [Synonyms]
[Rh(coe)2Cl]2
Chlorobis(cyclooctene)rhodium(I)
CHLOROBIS(CYCLOOCTENE)RHODIUM()DIMER
Chlorobis(cyclooctene)rhodium(I)dimere
CHLOROBIS(CYCLOOCTENE)RHODIUM(I) DIMER
Chlorobis(cyclooctene)rhodiuM(I),diMer 98%
Chlorobis(cyclooctene)rhodium(I) dimer,98%
Chlorobis(cyclooctene)rhodium(I)dimer,min.98%
Chlorobis(cyclooctene)rhodium(I) dimer, min. 98%
Chlorobis(cyclooctene)rhodiuM(I) diMer, 98% 100MG | [EINECS(EC#)]
623-340-7 | [Molecular Formula]
C32H56Cl2Rh2 | [MDL Number]
MFCD00013287 | [MOL File]
12279-09-3.mol | [Molecular Weight]
717.5 |
| Chemical Properties | Back Directory | [Appearance]
orange-brown powder | [Melting point ]
190 °C (dec.)(lit.)
| [storage temp. ]
Freezer | [form ]
crystal | [color ]
orange to red | [Sensitive ]
air sensitive, store cold | [CAS DataBase Reference]
12279-09-3 |
| Hazard Information | Back Directory | [Chemical Properties]
orange-brown powder | [Uses]
Chlorobis(cyclooctene)rhodium(I),dimer can be used as a catalyst:
- To synthesize enantioenriched gem-diaryl sulfonates by asymmetric 1,4-addition of aryl boronic acids to α,β-unsaturated sulfonyl compounds.
- In direct C-arylation of N-unprotected indoles and pyrroles.
- In the carboxylation of arenes via C-H bond activation.
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