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2-iodo-N-methoxy-N,5-dimethylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1262282-36-9

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1262282-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262282-36-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,2,8 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1262282-36:
(9*1)+(8*2)+(7*6)+(6*2)+(5*2)+(4*8)+(3*2)+(2*3)+(1*6)=139
139 % 10 = 9
So 1262282-36-9 is a valid CAS Registry Number.

1262282-36-9Relevant academic research and scientific papers

Weinreb Amide Directed Versatile C?H Bond Functionalization under (η5-Pentamethylcyclopentadienyl)cobalt(III) Catalysis

Kawai, Kentaro,Bunno, Youka,Yoshino, Tatsuhiko,Matsunaga, Shigeki

supporting information, p. 10231 - 10237 (2018/07/29)

The (η5-pentamethylcyclopentadienyl)cobalt(III) (Cp*CoIII)-catalyzed C?H bond functionalization of aromatic, heteroaromatic, and α,β-unsaturated Weinreb amides was explored. C?H allylation reactions with the use of allyl carbonate and a perfluoroalkene, oxidative alkenylation reactions with the use of ethyl acrylate, iodination reactions with the use of N-iodosuccinimide, and amidation reactions with the use of dioxazolones were catalyzed by Cp*Co(CO)I2 in the presence of a cationic Ag salt and AgOAc to afford various synthetically useful building blocks. Mechanistic studies of the C?H allylation disclosed that the C?H activation step was rate determining and virtually irreversible.

Copper(II)chloride-mediated cyclization reaction of N-alkoxy- orthoalkynylbenzamides

Jithunsa, Manita,Ueda, Masafumi,Miyata, Okiko

supporting information; experimental part, p. 518 - 521 (2011/04/16)

A regioselective intramolecular cyclization/halogenation reaction of N-alkoxy-o-alkynylbenzamides with CuCl2/NCS was developed. The corresponding 3-(chloromethylene)isobenzofuran-1-ones were exclusively obtained via 5-exo-dig cyclization in moderate to excellent yields within 0.5-1 h. This approach has been successfully used to synthesize a biaryl compound by the Suzuki-Miyaura reaction.

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