Bis(triphenylphosphine)rhodium(I) carbonyl chloride
95%
- Product Code: 68468
Alias:
Bis(triphenylphosphine)carbonyl rhodium(I) chloride, triphenylphosphinecarbonyl rhodium chloride, bis(triphenylphosphine)carbonyl rhodium(I) chloride
CAS:
13938-94-8
| Molecular Weight: | 690.94 g./mol | Molecular Formula: | C₃₇H₃₀ClOP₂Rh |
|---|---|---|---|
| EC Number: | 237-712-8 | MDL Number: | MFCD00044273 |
| Melting Point: | 224-227 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Bis(triphenylphosphine)rhodium(I) carbonyl chloride is widely used as a catalyst in various organic synthesis reactions. It plays a crucial role in hydrogenation processes, particularly in the reduction of alkenes, alkynes, and carbonyl compounds to their corresponding saturated forms. This compound is also employed in hydroformylation reactions, where it facilitates the conversion of alkenes into aldehydes, a key step in the production of alcohols and other derivatives. Additionally, it is utilized in carbonylation reactions, enabling the insertion of carbon monoxide into organic molecules to form esters, acids, or amides. Its effectiveness in these catalytic processes makes it valuable in the pharmaceutical and fine chemical industries for the synthesis of complex molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow powder or crystals |
| ICP MAJOR ANALYSIS CONFIRMED | CONFIRMS RH AND P COMPONENTS |
| INFRARED SPECTROMETRY | Conforms to Structure |
| RHODIUM | 14.45 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $266.43 |
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| 1.000 | 10-20 days | $678.07 |
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Bis(triphenylphosphine)rhodium(I) carbonyl chloride
Bis(triphenylphosphine)rhodium(I) carbonyl chloride is widely used as a catalyst in various organic synthesis reactions. It plays a crucial role in hydrogenation processes, particularly in the reduction of alkenes, alkynes, and carbonyl compounds to their corresponding saturated forms. This compound is also employed in hydroformylation reactions, where it facilitates the conversion of alkenes into aldehydes, a key step in the production of alcohols and other derivatives. Additionally, it is utilized in carbonylation reactions, enabling the insertion of carbon monoxide into organic molecules to form esters, acids, or amides. Its effectiveness in these catalytic processes makes it valuable in the pharmaceutical and fine chemical industries for the synthesis of complex molecules.
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