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N-(p-anisyl)furan-2-carboxyimidoyl chloride is a chemical compound with the molecular formula C12H8ClNO3. It is a derivative of furan-2-carboxylic acid, featuring a p-anisyl group (a phenyl ring with a methoxy group at the para position) attached to the nitrogen atom of the imidoyl chloride functional group. N-(p-anisyl)furan-2-carboxyimidoyl chloride is often used as a reagent in organic synthesis, particularly in the formation of amide bonds and as a protecting group in peptide synthesis. Its structure allows for versatile chemical reactions, making it a valuable tool in the field of chemistry.

6436-31-3

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6436-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6436-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6436-31:
(6*6)+(5*4)+(4*3)+(3*6)+(2*3)+(1*1)=93
93 % 10 = 3
So 6436-31-3 is a valid CAS Registry Number.

6436-31-3Relevant academic research and scientific papers

Domino 1,4- And 1,6-Addition Reactions of Ketene Silyl Acetals to Dialkynyl Imines Promoted by Aluminum Chloride: Synthesis of Multifunctionalized β-Lactams

Hachiya, Iwao,Nakamura, Kenta,Hara, Masaya,Sato, Koki,Shimizu, Makoto

, p. 14770 - 14794 (2019)

Domino 1,4- and 1,6-addition reactions of ketene silyl acetals to dialkynyl imines are disclosed. Aluminum chloride promoted domino 1,4- and 1,6-addition reactions of ketene silyl acetals to dialkynyl imines to give a variety of alkenyl iminocyclobutenones in moderate to good yields. The chemoselective reduction of alkenyl iminocyclobutenones and the subsequent thermal rearrangement of resulting alkenyl aminocyclobutenones in the presence of appropriate amines provided cis or trans multifunctionalized β-lactams in moderate to high yields with good to high diastereoselectivities.

Catalytic hydrogenation of α-iminophosphonates as a method for the synthesis of racemic and optically active α-aminophosphonates

Goulioukina, Nataliya S.,Bondarenko, Grigorii N.,Lyubimov, Sergey E.,Davankov, Vadim A.,Gavrilov, Konstantin N.,Beletskaya, Irina P.

experimental part, p. 482 - 492 (2009/04/10)

It was shown that the catalytic hydrogenation of α-iminophosphonates by molecular hydrogen can serve as a convenient method for the synthesis of racemic and optically active α-aminophosphonates. Up to 94% ee was achieved in the rhodium-catalyzed enantiose

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