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Benzenecarboximidic acid, butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35590-19-3

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35590-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35590-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35590-19:
(7*3)+(6*5)+(5*5)+(4*9)+(3*0)+(2*1)+(1*9)=123
123 % 10 = 3
So 35590-19-3 is a valid CAS Registry Number.

35590-19-3Relevant academic research and scientific papers

Synthesis of Functionalized Indenones via Rh-Catalyzed C-H Activation Cascade Reaction

Lv, Ningning,Chen, Zhengkai,Liu, Yue,Liu, Zhanxiang,Zhang, Yuhong

, p. 2588 - 2591 (2017)

An efficient and expeditious protocol for the synthesis of diverse difunctionalized indenones through rhodium-catalyzed C-H activation and multistep cascade reaction of benzimidates and alkenes has been developed. The transformation involves the cleavage and formation of multiple bonds in one pot under mild reaction conditions, and Mn(OAc)2 plays an important role in the reaction.

Cobalt-Catalyzed Oxidant-Free Spirocycle Synthesis by Liberation of Hydrogen

Lv, Ningning,Liu, Yue,Xiong, Chunhua,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 4640 - 4643 (2017/09/12)

The first example of oxidant-free cobalt-catalyzed synthesis of five-membered spirocycles is reported from benzimidates and maleimides utilizing nitrobenzene as promoter. In contrast to previously known cobalt-catalyzed oxidative C-H functionalization rea

Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis

Wang, Qiang,Li, Xingwei

supporting information, p. 2102 - 2105 (2016/06/01)

Nitrosobenzenes have been used as a convenient aminating reagent for the efficient synthesis of 1H-indazoles via rhodium and copper catalyzed C-H activation and C-N/N-N coupling. The reaction occurred under redox-neutral conditions with high efficiency and functional group tolerance. Moreover, a rhodacyclic imidate complex has been identified as a key intermediate.

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