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CAS RN: 17185-29-4 | Product Number: C1383
Carbonylhydridotris(triphenylphosphine)rhodium(I)
Purity:
Synonyms:
- Carbonyltris(triphenylphosphine)rhodium(I) Hydride
- Tris(triphenylphosphine)rhodium(I) Carbonyl Hydride
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information |
---|---|---|---|---|---|
1G |
$200.00
|
4 | 0 | Contact Us | |
5G |
$773.00
|
27 | 4 | Contact Us |
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Product Number | C1383 |
Molecular Formula / Molecular Weight | C__5__5H__4__6OP__3Rh = 918.80 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Moisture Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 17185-29-4 |
PubChem Substance ID | 87566394 |
SDBS (AIST Spectral DB) | 39303 |
Merck Index (14) | 9758 |
MDL Number | MFCD00151644 |
Specifications
Appearance | Light yellow to Yellow powder to crystal |
Elemental analysis(Carbon) | 70.50 to 72.60 % |
Properties (reference)
Melting Point | 122 °C(dec.) |
Solubility (soluble in) | Chloroform, dichloromethane, Benzene |
GHS
Hazard Statements | H413 : May cause long lasting harmful effects to aquatic life. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. |
Related Laws:
Transport Information:
H.S.code* | 2843.90-000 |
Application
Rh(I)-catalyzed synthesis of indoles through the amino-Claisen rearrangement of N-propargylanilines
Typical procedure: Under an argon atmosphere, to a solution of carbonyltris(triphenylphosphine)rhodium(I) hydride (16 micro-mol) in 1,1,1,3,3,3-hexafluoro-2-propanol (1 mL) is added N-2-butynyl-N-benzyl-4-methoxyaniline (0.4 mmol) in 1,1,1,3,3,3-hexafluoro-2-propanol (1.5 mL) at an ambient temperature, and the mixture is refluxed until the consumption of the substrate by TLC analysis. The mixture is diluted with ether and filtered through a Celite pad. After concentration of the filtrate to dryness, purification by silica gel chromatography (hexane/AcOEt = 25:1) gives the corresponding indole in 99% yield.
References
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