| Identification | Back Directory | [Name]
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate | [CAS]
99326-34-8 | [Synonyms]
Bis(1,5-cyclooctadie
Bis(1,5-cyclooctadiene)
Bis(1,5-cyclooctadiene)rhodium triflate
BIS(1,5-CYCLOOCTADIENE)RHODIUM(I) TRIFL&
Bis(1,5-cyclooctadiene)rhodium(I) triflate
BIS(1,5-CYCLOOCTADIENE)RHODIUM(I)TRIFLUOROMETHANESULFONATE
BIS(1,5-CYCLOOCTADIENE)-TRIFLUOROMETHANESULFITORHODIUM (I)
Bis-(1,5-cyclooctadiene)-rhodium trifluoromethanesulfonate
Bis(1,5-cyclooctadiene)rhodium(Ⅰ) trifluoromethanesulfonate
Bis(1,5-cyclooctadiene)rhodium(I)trifluoromethanesulphonate99%
Bis(1,5-cyclooctadiene)rhodium(I)trifluoromethanesulfonate,99%
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate,97%
Bis(1,5-cyclooctadiene)rhodiuM(I) trifluoroMethanesulfonate 98%
1,5-Cyclooctadiene(hydroquinone)rhodiuM(I) tetrafluoroborate,98%
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethane sulphonate 99%
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethane sulphonate 98+% | [Molecular Formula]
C17H24F3O3RhS | [MDL Number]
MFCD00143752 | [MOL File]
99326-34-8.mol | [Molecular Weight]
468.34 |
| Chemical Properties | Back Directory | [Appearance]
dark red crystals | [Melting point ]
159 °C (dec.)(lit.)
| [storage temp. ]
Refrigerator (+4°C) | [solubility ]
Soluble in chloroform | [form ]
crystal | [color ]
dark red | [Water Solubility ]
insoluble | [Sensitive ]
Air Sensitive | [Exposure limits]
ACGIH: TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 0.1 mg/m3 | [InChI]
1S/2C8H12.CHF3O3S.Rh/c2*1-2-4-6-8-7-5-3-1;2-1(3,4)8(5,6)7;/h2*1-2,7-8H,3-6H2;(H,5,6,7);/q;;;+1/p-1/b2*2-1-,8-7-;; | [InChIKey]
GOPBTCMAUMSOBX-QMDOQEJBSA-M | [SMILES]
[Rh+].[O-]S(=O)(=O)C(F)(F)F.C1CC=CCCC=C1.C2CC=CCCC=C2 |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26 | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [TSCA ]
No | [HS Code ]
28439000 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2 |
| Questions And Answer | Back Directory | [Reaction]
- Rhodium catalyzed contrasteric regiocontrolled hydrogenative couplings of nonsymmetric 1,3-diynes to ethyl glyoxalate
- Rhodium catalyzed reductive Mannich coupling of vinyl ketones to N-Sulfonylimines mediated by hydrogen
- Rhodium catalyzed asymmetric synthesis of Sitagliptin
- Rhodium catalyzed asymmetric hydrogenation of tetrasubstituted α,β-unsaturated ketones
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