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CAS RN: 15956-28-2 | 產品號碼: R0069
Rhodium(II) Acetate Dimer
包裝 | 價格 | 同一天 | 2-3个工作日 |
---|---|---|---|
100MG |
NT$5,800
|
8 | 32 |
1G |
NT$31,960
|
10 | ≥40 |
* 以上價格已含運費關稅等但一些需要海運以及乾冰運輸的產品除外,詳情請與
當地經銷商
洽詢。
* TCI會時常優化儲存條件,儲存溫度請以在線目錄為準,敬請留意。
產品號碼 | R0069 |
分子式 / 分子量 | C__8H__1__2O__8Rh__2 = 441.99 |
外觀與形狀(20°C) | Solid |
儲存條件 | Room Temperature (Recommended in a cool and dark place, <15°C) |
包裝和容器 | 100MG-Glass Bottle with Plastic Insert (閲覽圖片), 1G-Glass Bottle with Plastic Insert (閲覽圖片) |
CAS RN | 15956-28-2 |
Reaxys-RN | 14201302 |
PubChem Substance ID | 87575627 |
MDL編號 | MFCD00003538 |
產品規格
Appearance | Green to Dark green powder to crystal |
Elemental analysis(Carbon) | 20.50 to 22.70 % |
性質
熔點 | 240 °C |
GHS
相關法規
RTECS # | VI9361000 |
運輸資料
HS編碼* | 2843.90-000 |
Application
One-pot Synthesis of Pyrroles from Terminal Alkynes, N-Sulfonyl Azides, and Alkenyl Alkyl Ethers
Typical Procedure:
Alkyne (0.2 mmol), TsN3 (1.0 eq.), alkenyl alkyl ether (3.0 eq.), CuTC (10.0 mol%), Rh2(OAc)4 (1.0 mol%), and DCE (0.2 M) are added to an oven-dried test tube under nitrogen atmosphere. The reaction mixture is stirred at ambient temperature for 3 h and then, heated at 80 °C for 4–13 h. After the reaction mixture is filtered through short path of celite with CH2Cl2, the filtrate is concentrated under reduced pressure. The residue is purified by silica gel column chromatography (ethyl acetate–hexane) to give pyrrole derivatives (Y. 65–81%).
Alkyne (0.2 mmol), TsN3 (1.0 eq.), alkenyl alkyl ether (3.0 eq.), CuTC (10.0 mol%), Rh2(OAc)4 (1.0 mol%), and DCE (0.2 M) are added to an oven-dried test tube under nitrogen atmosphere. The reaction mixture is stirred at ambient temperature for 3 h and then, heated at 80 °C for 4–13 h. After the reaction mixture is filtered through short path of celite with CH2Cl2, the filtrate is concentrated under reduced pressure. The residue is purified by silica gel column chromatography (ethyl acetate–hexane) to give pyrrole derivatives (Y. 65–81%).
References
Application
Highly Diastereoselective Synthesis of Fully Substituted Tetrahydrofurans
Typical Procedure: A flask is charged with allyl alcohol (0.10 mmol, 1.0 eq.), Rh2(OAc)4 (2.0 mol%) and 4A MS (0.1 g) in toluene (1.5 mL), the reaction mixture is stirred at 45℃, and a solution of the diazo compound (0.20 mmol) in toluene (0.5 mL) is added to the reaction mixture over a period of 1 h through a syringe pump. After completion of the addition, piperidine (2.0 eq.) is added and the reaction mixture is stirred for additional 5-10 h (reaction completion is monitored by TLC) at 45℃. The reaction mixture is purified by flash chromatography on silica gel (EtOAc : light petroleum ether = 1 : 50 to 1 : 20) to give the pure product.
References
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