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Burgess reagent sds

WebMSDS: Download: Burgess reagent Burgess reagent is a term used to describe Methyl N-(triethylammoniumsulphonyl) carbamate. It is a selective agent of mild strength used for dehydration in organic reactions and synthesis. Its main use … 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 ...

Burgess reagent Safety Data Sheets(SDS) lookchem

WebThe Burgess reagent is a commercially available compound that has historically found utility as a dehydrating agent. The reagent may also be used to oxidize primary and secondary alcohols to their corresponding aldehydes and ketones in dimethyl sulfoxide. These oxidations were found to be rapid under mild conditions. WebJul 15, 2024 · We provide Ethanaminium, N,N-diethyl-N-[[(methoxycarbonyl)amino]sulfonyl]-, inner salt safety data sheet view and download for free at Echemi.com. Product. ... eazycity avis https://htctrust.com

1196145-01-3 Benzyl 3-amino-4-oxopiperidine-1-carboxylate …

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. WebAug 11, 2024 · Burgess reagent SDS Post Buying Request. SAFETY DATA SHEETS According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition. Version: 1.0. Creation Date: Aug 11, 2024. Revision Date: Aug 11, 2024. 1. Identification 1.1 GHS Product identifier. WebJul 16, 2024 · Burgess-type reagents provide tremendous utility in organic synthesis but see limited use on large scales because of their high cost and instability. Nevertheless, extensive process development led to a scale-friendly process where in situ formation of a Boc-Burgess reagent enabled access to a chiral cyclic sulfamate from inexpensive … company in wtc

AK Scientific, Inc. Page 1 of 5 Safety Data Sheet (United …

Category:Burgess reagent, (Methoxycarbonylsulfamoyl)triethylammonium hydroxide

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Burgess reagent sds

(Methoxycarbonylsulfamoyl)triethylammonium hydroxide …

WebBurgess reagent: Alt. name : Methyl N-(triethylammoniosulfonyl)carbamate : CAS number : 29684-56-8: Related CAS : MFCD number : MFCD00077815: Purity : 95% : Formula : … WebSynonym (s): Burgess reagent, Methyl N- (triethylammoniosulfonyl)carbamate Linear Formula: CH3O2CNSO2N (C2H5)3 CAS Number: 29684-56-8 Molecular Weight: 238.30 …

Burgess reagent sds

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WebBurgess reagent CAS 29684-56-8 SDS including Hazard identification, Composition/information on ingredients, First-aid measures, Fire-fighting measures, …

WebSafety Data Sheet acc. to OSHA HCS Printing date 01/23/2014 Reviewed on 01/24/2007 Product name: Burgess Reagent (Contd. of page 5) 38.0.2 Data Sheet, or in combination with any other product or process, is the responsibility of the user. Department issuing SDS: Health, Safety and Environmental Department. Abbreviations and acronyms: WebSAFETY DATA SHEET Creation Date 26-Sep-2009 Revision Date 19-Feb-2024 Revision Number 1 1. Identification Product Name Burgess Reagent Cat No. : L20155 CAS-No …

WebSafety Data Sheet acc. to OSHA Hazard Communication Standard (29 CFR 1910.1200) Printing date 03/05/2015 Reviewed on 11/29/2014 40.0 1 Identification · Product identifier · Trade name:Burgess Reagent · Article number:220535 · CAS Number: 29684-56-8 · Application of the substance / the mixtureLaboratory chemicals for research and … WebProduct name: Burgess Reagent Catalog#: M130 IUPAC name: Methoxy{[(triethylammonio)sulfonyl]imino}methanolate Product use restrictions: Only for …

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 ...

WebDec 24, 2024 · Product name: Burgess reagent; CBnumber: CB2152668; CAS: 29684-56-8; EINECS Number: 629-648-8; Synonyms: burgess,Burgess reagent; Relevant … eazycity corkWebSDS. Alternatived Products of [ 1196145-01-3 ] Product Details of [ 1196145-01-3 ] CAS No. : 1196145-01-3: MDL No. : MFCD12756125: Formula : C 13 H 17 ClN 2 O 3: ... Multi-step reaction with 7 steps 1: triethylamine / dichloromethane / 3 h / 0 °C 2: Burgess Reagent / tetrahydrofuran / 0.5 h / 120 °C 3: palladium on activated charcoal ... eazyclean technologies gmbhWebThe Burgess reagent is a commercially available compound that has historically found utility as a dehydrating agent. The reagent may also be used to oxidize primary and … eazy chair xlWebMay 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。 eazy cleaningWebGrignard reagents are highly reactive organomagnesium halides formed by the reaction of magnesium metal with alkyl or alkenyl halides. They are very strong bases and react with acidic hydrogens such as alcohols, water and carboxylic acids. Our comprehensive portfolio of Grignard reagents, used in the Grignard reaction to form new carbon-carbon bonds, … eazy cash stanbicWebSafety Data Sheet per OSHA HazCom 2012 38.0.2 1 Identification Product identifier Product name: Burgess Reagent Stock number: L20155 CAS Number: 29684-56-8 Relevant identified uses of the substance or mixture and uses advised against. Identified use: SU24 Scientific research and development Details of the supplier of the safety data … eazycheatsWebThe 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 company ip finder