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1H-Imidazole-4,5-dicarbonitrile, 2-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63857-93-2

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63857-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63857-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63857-93:
(7*6)+(6*3)+(5*8)+(4*5)+(3*7)+(2*9)+(1*3)=162
162 % 10 = 2
So 63857-93-2 is a valid CAS Registry Number.

63857-93-2Downstream Products

63857-93-2Relevant academic research and scientific papers

CuOx/OMS-2 catalyzed synthesis of 4,5-dicyano-1H-imidazoles moiety: Directly access to D-A system for AIE-active mechanofluorochromic materials

Zheng, Kaibo,Chen, Hui,Xiao, Yufeng,Yan, Jiaying,Zhang, Nuonuo,Liu, Xiang

, (2021/11/16)

Although a lot of mechanofluorochromic (MFC) materials have been reported, it still needs to be further explored due to the lack of the universal design principle. The AIE moiety molecules with D-A framework have been widely regarded as the ideal structur

Rapid synthesis of 2-amino maleonitrile Schiff bases in aqueous media catalyzed by cerium(IV) ammonium nitrate (CAN) and a new method for the one-pot preparation of their dicyano imidazoles (DCI)

Kalhor, Mehdi,Seyedzade, Zahra

, p. 3349 - 3360 (2017/04/19)

A quick and simple method has been developed for the synthesis of 2-amino maleonitrile Schiff bases 3(a–k) through the reaction of 2,3-diaminomaleonitrile (DAMN) and aromatic aldehydes in the presence of catalytic amounts of cerium(IV) ammonium nitrate (C

Imidazoles and their compositions for plant growth regulation

-

, (2008/06/13)

The invention provides a method of regulating the growth of a plant using a compound of the formula: wherein R1 represents alkyl or phenyl optionally substituted by halogen, alkyl, alkoxy, alkylthio, trifluoromethyl, trifluoromethoxy, trifluoromethylthio,

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