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Cyclohexanecarboxamide, N-(2-bromophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

378786-43-7

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378786-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 378786-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,8,7,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 378786-43:
(8*3)+(7*7)+(6*8)+(5*7)+(4*8)+(3*6)+(2*4)+(1*3)=217
217 % 10 = 7
So 378786-43-7 is a valid CAS Registry Number.

378786-43-7Relevant academic research and scientific papers

Pd-Catalyzed Carbonylative Synthesis of 4H-Benzo[d][1,3]Oxazin-4-Ones Using Benzene-1,3,5-Triyl Triformate as the CO Source

Zheng, Yan,Dong, Mengke,Qu, Erdong,Bai, Jin,Wu, Xiao-Feng,Li, Wanfang

supporting information, p. 16219 - 16224 (2021/10/06)

A facile synthesis of 4H-benzo[d][1,3]oxazin-4-one derivatives by Pd-catalyzed carbonylative cross-coupling between N-(ortho-bromoaryl)amides and benzene-1,3,5-triyl triformate (TFBen) was developed. This procedure does not require the toxic and flammable gas CO as the carbonyl source and tolerates a wide scope of functional groups. Remarkably, 4H-benzo[d][1,3]oxazin-4-ones incorporated to natural products and drugs can be constructed by this method.

Base-catalyzed synthesis of aryl amides from aryl azides and aldehydes

Xie, Sheng,Zhang, Yang,Ramstr?m, Olof,Yan, Mingdi

, p. 713 - 718 (2015/12/30)

Aryl amides have been used as important compounds in pharmaceuticals, materials and in molecular catalysis. The methods reported to prepare aryl amides generally require very specific reagents, and the most popular carboxyl-amine coupling reactions demand stoichiometric activators. Herein, we report that aryl azides react with aldehydes under base-catalyzed conditions to yield aryl amides efficiently. Mechanistic investigations support the formation of triazoline intermediates via azide-enolate cycloaddition, which subsequently undergo rearrangement to give amides by either thermal decomposition (20-140 °C) or aqueous acid work-up at room temperature. The strategy does not require nucleophilic anilines and is especially efficient for highly electron-deficient aryl amides, including perfluoroaryl amides, which are otherwise challenging to synthesize.

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