Antihypertensive drugs

(-)-1-(9-Fluorenyl)ethyl chloroformate is mostly used as an in-capillary derivatization agent for the separation of amino acid (AA) derivatives by micellar electrokinetic chromatography (MEKC).

(-)-3-(3,4-Dihydroxyphenyl)-2-methyl-L-alanine sesquihydrate

Application Both (+)- and (-)-DIP-chloride are used for asymmetric reduction of prochiral ketones and for the preparation of &#946 -amino alcohols. Reagent used for an enantioselective reduction of (chloroacetyl) benzofurans to chlorohydrins which

Application Both (+)- and (-)-DIP-chloride are used for asymmetric reduction of prochiral ketones and for the preparation of &#946 -amino alcohols. Reagent used for an enantioselective reduction of (chloroacetyl) benzofurans to chlorohydrins which

Application Both (+)- and (-)-DIP-chloride are used for asymmetric reduction of prochiral ketones and for the preparation of &#946 -amino alcohols. Reagent used for an enantioselective reduction of (chloroacetyl) benzofurans to chlorohydrins which

(&#8722)-DIP-Chloride &#8482 solution is a pinane-based asymmetric reducing agent that is commonly used in asymmetric reduction reactions. Application (&#8722)-Diisopinocampheylchloroborane [(&#8722)-DIP-Chloride &#8482 ] solution can be used

(&#8722)-DIP-Chloride &#8482 solution is a pinane-based asymmetric reducing agent that is commonly used in asymmetric reduction reactions. Application (&#8722)-Diisopinocampheylchloroborane [(&#8722)-DIP-Chloride &#8482 ] solution can be used

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

(&#8722)-Gallocatechin gallate is a polyphenolic compound having a galloyl moiety. It is an epimerized form of epigallocatechin gallate, which is common tea catechin.

Analysis Note Assay (acidimetric): &#8805 99.0 % Spec.

Analysis Note Assay (acidimetric): &#8805 99.0 % Spec.

Other Notes Treating this chlorosilane with sec-BuLi gives 1-chloro-1-trimethylsilylethyl lithium which reacts with aldehydes and ketones to form methyl ketones via an intermediate &#945,&#946-epoxysilane. Used in an efficient synthesis of