Search
項目搜尋
結構搜尋
Thermo Scientific Chemicals
3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals
| 產品號碼 | Quantity |
|---|---|
| H52989.03 亦稱為 H52989-03 | 1 g |
規格
CAS871332-96-6
Chemical Name or Material3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid
Formula Weight233.98
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
檢視更多
Reactant involved in suzuki-miyaura cross-coupling reactions, aerobic oxidative cross-coupling, rhodium-catalyzed addition reactions.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Reactant involved in suzuki-miyaura cross-coupling reactions, aerobic oxidative cross-coupling, rhodium-catalyzed addition reactions.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents. Store at 4°C.
Reactant involved in suzuki-miyaura cross-coupling reactions, aerobic oxidative cross-coupling, rhodium-catalyzed addition reactions.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents. Store at 4°C.
RUO – Research Use Only
General References:
- Masafumi Ueda et. al. Palladium-catalyzed cross coupling reaction of N-alkoxyimidoyl bromides and its application to one-pot synthesis of N-arylamines.. Chemical & Pharmaceutical Bulletin,. 2011, 59 (9), 1206-1208 .
- Feng Xue et. al. A class of benzene backbone-based olefin-sulfoxide ligands for Rh-catalyzed enantioselective addition of arylboronic acids to enones.. Journal of Organic Chemistry, 2011, 76 (17), 7256-7262.