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1,1-dimethyl-n-(1-phenylethylidene)ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40475-58-9

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40475-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40475-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,7 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40475-58:
(7*4)+(6*0)+(5*4)+(4*7)+(3*5)+(2*5)+(1*8)=109
109 % 10 = 9
So 40475-58-9 is a valid CAS Registry Number.

40475-58-9Relevant academic research and scientific papers

Synthesis and Properties of Some Nitroxide α-Carboxylate Salts

Keana, John F. W.,Sovitj, Pou,Rosen, Gerald M.

, p. 2417 - 2420 (1989)

Nitroxide α-carboxylates 10 and 22a-e were synthesized for evaluation as potential contrast-enhancing agents for magnetic resonance imaging applications.While pyrrolidine nitroxide carboxylate 10 was stable indefinitely, the free acid form 11 could not be

Synthesis of 4-Isoxazolines via Visible-Light Photoredox-Catalyzed [3 + 2] Cycloaddition of Oxaziridines with Alkynes

Jang, Gwang Seok,Lee, Junggeun,Seo, Jungseok,Woo, Sang Kook

supporting information, p. 6448 - 6451 (2017/12/08)

A method for [3 + 2] cycloaddition of oxaziridines with alkynes to form 4-isoxazolines via visible-light photoredox catalysis is described. This method is a greener, atom-economical reaction that tolerates various functional groups and provides good to excellent yield. Moreover, the cyclization products can be conveniently converted into tetrasubstituted allylic alcohols and enamines. A mechanistic study suggests that the reaction involves photoredox-catalyzed in situ generation of a nitrone from the oxaziridine by SET.

Internal adduct formation of active intramolecular C4-bridged frustrated phosphane/borane Lewis pairs

Wang, Xiaowu,Kehr, Gerald,Daniliuc, Constantin G.,Erker, Gerhard

supporting information, p. 3293 - 3303 (2014/03/21)

The tetramethylene-bridged PMes2/B(C6F 5)2 frustrated Lewis pair (FLP) 8 was prepared by hydroboration of Mes2P-(CH2)2CH=CH2 with HB(C6F5)2. It is an active FLP that splits dihydrogen under mild conditions and, consequently, serves as a metal-free hydrogenation catalyst for a variety of substrates. It also reacts typically with terminal acetylenes. The C4-bridged FLP 23 was prepared by HB(C6F5)2 hydroboration of 1- dimesitylphosphino-2-vinylferrocene. It represents a rare example of a FLP where the equilibrium between the open form and the closed internal P/B adduct form is experimentally observable. It also shows a variety of typical FLP reactions, including dihydrogen splitting. The FLPs 8 and 23 (open form) and many precursors and products were characterized by X-ray diffraction.

Modular synthesis of indoles from imines and o-dihaloarenes or o-chlorosulfonates by a Pd-catalyzed cascade process

Barluenga, Jose,Jimenez-Aquino, Agustin,Aznar, Fernando,Valdes, Carlos

supporting information; experimental part, p. 4031 - 4041 (2009/09/04)

A detailed study of the scope of a new Pd-catalyzed synthesis of indolesfrom 1,2-dihaloarenes and o-halobenzene sulfonates and imines is descri bed. The cascade reaction comprises an imine a-arylation ollowed by an intramolecular C-N bond-forming reaction promoted by the same Pd catalyst. The reaction with 1,2-dibromobenzene shows wide scope and allows the introduction of aryl, alkyl, and vinyl substituents at different positions of the five-membered ring of the indole. The regioselective synthesis of indoles substituted in the six-membered ring can be carried out by employing o-dihalobenzene derivatives with two different halogens, taking advantage of the different reactivities of I, Br, and Cl in oxidative addition reactions. This paper also introduces a method for the efficient cleavage of the N-t-butyl group, thus allowing for the preparation of N-H indoles through the same methodology. Finally, the reaction with o-halosulfonates has been studied. The best substrates are o-chlorononaflates, which lead to indoles in very high yield. The reaction is particularlyappropriate for the synthesis of the challenging 6-substituted indoles. In view of the availability of o-chlorophenols, which are direct precur sors of the chlorononaflates, this reaction represents an efficient entry into indoles substituted in the six-membered ring. The concept is illustrated by the preparation of a 4,6-disubstituted indole from naturally occurring anethole.

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