3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals
3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals
3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals

製品番号(カタログ番号)数量
H52989.03
または、製品番号H52989-03
1 g
製品番号(カタログ番号) H52989.03
または、製品番号H52989-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
仕様
CAS871332-96-6
化学物質名または材質3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid
式量233.98
健康被害1H315-H319-H335
健康被害2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
さらに表示
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.
RUO – Research Use Only

General References:

  1. 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 .
  2. 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.