WebDescription. Burgess reagent is a selective dehydrating reagent used in organic synthesis. It is used to convert secondary and tertiary alcohol, with an adjacent proton, into alkenes. Burgess reagent is also utilized to promote great synthetic values in medicinal chemistry. It has been used in dehydration of primary amides, formamides and ... WebThe Burgess reagent is a carbamate and used for the dehydration of various sec- and tert- alcohols to get the corresponding olefins. Moreover, it also found applications in numerous synthetic transformations in organic chemistry and particularly in medicinal chemistry. Applications of Burgess Reagent in Synthetic organic Chemistry
SAFETY DATA SHEET Revision Date 09/18/2024 …
WebDescription. Burgess reagent is a selective dehydrating reagent used in organic synthesis. It is used to convert secondary and tertiary alcohol, with an adjacent proton, into alkenes. Burgess reagent is also utilized to … WebSAFETY DATA SHEET Creation Date 28-Nov-2012 Revision Date 08-Mar-2024 Revision Number 8 1. Identification Product Name Griess Reagent Cat No. : AC328670000; AC328670500 Synonyms No information available Recommended Use Laboratory chemicals. Uses advised against Food, drug, pesticide or biocidal product use. Details of … complete the trial path eso
Burgess reagent Safety Data Sheets(SDS) lookchem
WebMay 31, 2024 · 艾美捷星形孢菌素Staurosporine (Stsp) 是来自大鼠脑的蛋白激酶 C (PKC) 的有效抑制剂,其 IC 50值为 2.7 nM。它对大鼠重组 PKC- α的抑制作用分别比 PKC- δ 和 PKC- ζ高约 100 倍和 1,000倍。 WebSafety Data Sheet acc. to OSHA HCS Printing date 05/25/2024 Reviewed on 05/20/2024 53.0.0.2 1 Identification · Product identifier · Trade name: Burgess Reagent · Article number: 220535 · CAS Number: 29684-56-8 · Application of the substance / the mixture Laboratory chemicals for research and development · Details of the supplier of the ... WebThe Burgess reagent ( methyl N- (triethylammoniumsulfonyl)carbamate) is a mild and selective dehydrating reagent often used in organic chemistry. [1] [2] It was developed in the laboratory of Edward M. Burgess at Georgia Tech . The Burgess reagent is used to convert secondary and tertiary alcohols with an adjacent proton into alkenes. ecchymotic tongue