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3,5-bis(methoxy)-N,N-dimethylbenzylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39727-93-0

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39727-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39727-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39727-93:
(7*3)+(6*9)+(5*7)+(4*2)+(3*7)+(2*9)+(1*3)=160
160 % 10 = 0
So 39727-93-0 is a valid CAS Registry Number.

39727-93-0Relevant academic research and scientific papers

Base-Mediated Borylsilylation/Silylation of Ammonium Salts with Silylborane

Du, Xian,Guan, Yun-Shi,Li, Yi-Hui,Liang, Guohai,Luo, Yong,Qi, Wan-Ying,Wang, Zi-Ying,Wei, Xun,Xu, Xiao-Hong,Yuan, Han,Zhen, Jing-Song

supporting information, p. 5988 - 5992 (2021/08/31)

This work describes a base-mediated borylsilylation of benzylic ammonium salts to synthesize geminal silylboronates bearing benzylic proton under mild reaction conditions. Deaminative silylation of aryl ammonium salts was also achieved in the presence of

Electrochemical Dehydrogenative Imidation of N-Methyl-Substituted Benzylamines with Phthalimides for the Direct Synthesis of Phthalimide-Protected gem-Diamines

Lian, Fei,Sun, Caocao,Xu, Kun,Zeng, Chengchu

supporting information, p. 156 - 159 (2019/01/11)

A general and green electrochemical dehydrogenative method for the imidation of N-methyl benzylamines with phthalimides with excellent regioselectivities is reported for the first time. This operationally simple method offers a valuable tool to obtain str

LiCl-Promoted Pd(ii)-catalyzed ortho carbonylation of N,N- dimethylbenzylamines

Li, Hu,Cai, Gui-Xin,Shi, Zhang-Jie

supporting information; experimental part, p. 10442 - 10446 (2011/01/08)

Palladium-catalyzed highly regioselective carbonylation of substituted N,N-dimethylbenzylamines with the assistance of LiCl was developed. The ortho-functionalized N,N-dimethylbenzylamine was further transformed into ortho-methyl benzoate under mild conditions. These two transformations could be combined into one pot to produce the desired product in moderate yield. Applications of this methodology to synthesize the fragments of variolaric acid were also studied.

Convenient Synthesis of Naturally Ocurring Methoxy- and Hydroxy Phthalides

Mali, R.S.,Jagtap, P.G.,Tilve, S.G.

, p. 2641 - 2652 (2007/10/02)

A convenient method for the synthesis of phthalides (1-5), involving heteroatom directed lithiation reaction is described.

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