Перейти к контенту
Main image
Печать
2-BROMOPHENYLBORONIC ACID, >=95.0%
Кат. №: 473804-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Печать
2-BROMOPHENYLBORONIC ACID, >=95.0%
Main image
Кат. №: 473804-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
2-BROMOPHENYLBORONIC ACID, >=95.0%
Кат. №: 473804-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description General description We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Find details here. Application Catalyzes the formation of amide bonds from amines and carboxylic acids. Used to promote greener amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents. Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect Packaging 5, 25 g in glass bottle Other Notes Contains varying amounts of anhydride
Related Categories
12 Principles Aligned Products, Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Greener Alternative Products, Greener Organometallics, Monosubstituted Aryl Boronic Acids, Organometallic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description General description We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Find details here. Application Catalyzes the formation of amide bonds from amines and carboxylic acids. Used to promote greener amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents. Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect Packaging 5, 25 g in glass bottle Other Notes Contains varying amounts of anhydride
Related Categories
12 Principles Aligned Products, Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Greener Alternative Products, Greener Organometallics, Monosubstituted Aryl Boronic Acids, Organometallic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.