Published TCIMAIL newest issue No.201
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| Product Number | U0141 |
Purity / Analysis Method
|
>90.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__6__1H__6__8Cl__2N__2Ru = 1,001.20 |
| Physical State (20 deg.C) | Solid |
Storage Temperature
|
Refrigerated (0-10°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive,Heat Sensitive |
| CAS RN | 2055540-61-7 |
| Reaxys Registry Number | 32783320 |
| PubChem Substance ID | 468593093 |
| MDL Number | MFCD31747049 |
| Appearance | Orange to Brown powder to crystal |
| Purity(HPLC) | min. 90.0 area% |
| NMR | confirm to structure |
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H371 : May cause damage to organs. H351 : Suspected of causing cancer. |
| Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P260 : Do not breathe dust. P202 : Do not handle until all safety precautions have been read and understood. P201 : Obtain special instructions before use. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection. P308 + P311 : IF exposed or concerned: Call a POISON CENTER/doctor. |
| HS Number | 2843909000 |
To a solution of diethyl diallylmalonate (0.240 mL, 0.99 mmol) in anhydrous toluene (9.8 mL) was added a solution of UltraCat (0.1 mol%, 0.001 mmol, 1.0 mg) in toluene (0.1 mL) in one shot. The mixture was stirred at 40 °C under nitrogen for 2 hours. To the reaction mixture, was added 1,4-bis(3-isocyanopropyl)piperazine (0.5 mol%, 1.0 mg) to deactivate the catalyst. The solvent was removed under reduced pressure to give a crude of 1 (0.187 g, 89%) as a deep orange oil. The residue was passed through silica gel (eluent: hexane) to obtain 1 (0.143 g, 68%) as a light yellow oil.
Toluene was dried over molecular sieves 4A and was degassed by purging with nitrogen before use.
Preparation of catalyst stock solution: UltraCat (5.0 mg) was dissolved in dry degassed toluene (0.5 mL).
The reaction mixture was analyzed by gas chromatography and the reaction completed within 30 min.
1H NMR (400 MHz, CDCl3); δ 5.60 (t, J =2.74 Hz, 2H), 4.20 (q, J =7.34 Hz, 4H), 3.01 (m, 4H), 1.25 (t, J=7.34 Hz, 4H).
13C NMR (101 MHz, CDCl3); δ 172.18, 127.75, 61.47, 58.78, 50.79, 13.98.
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