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2,3-bis-(2-fluorophenyl)quinoxaline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1389394-80-2

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1389394-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1389394-80-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,9,3,9 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1389394-80:
(9*1)+(8*3)+(7*8)+(6*9)+(5*3)+(4*9)+(3*4)+(2*8)+(1*0)=222
222 % 10 = 2
So 1389394-80-2 is a valid CAS Registry Number.

1389394-80-2Downstream Products

1389394-80-2Relevant academic research and scientific papers

SUBSTITUTED QUINOXALINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR4

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Page/Page column 47, (2014/08/20)

The present invention relates to novel quinoxaline derivatives of formula (I) as positive allosteric modulators for modulating metabotropic glutamate receptor subtype 4 (mGluR4) and/or altering glutamate level or glutamatergic signalling.

Pd(OAc)2-catalyzed regioselective aromatic C-H bond fluorination

Lou, Shao-Jie,Xu, Dan-Qian,Xia, Ai-Bao,Wang, Yi-Feng,Liu, Yun-Kui,Du, Xiao-Hua,Xu, Zhen-Yuan

supporting information, p. 6218 - 6220 (2013/07/25)

A novel Pd(OAc)2-NFSI-TFA system was developed for the highly selective ortho-monofluorination directed by diverse aryl-N-heterocyclic directing groups e.g., quinoxaline, pyrazole, benzo[d]oxazole, and pyrazine derivatives. A Pd(ii/iv) catalytic cycle was proposed based on the ESI-MS/MS studies. The Royal Society of Chemistry 2013.

One-pot synthesis of quinoxalines starting from aldehydes under metal-free conditions

Hu, Zhong-Yuan,Du, Ding,Tang, Wei-Fang,Lu, Tao

experimental part, p. 2262 - 2264 (2012/08/07)

An efficient and convenient synthesis of quinoxalines from easily available aldehydes was performed as a one-pot procedure in good to excellent yields under metal-free conditions, via sequential benzoin condensation, aerobic formation of benzils and condensation of the latter with 1,2-diaminobenzenes.

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