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Furan, 3-fluoro-2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31491-37-9

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31491-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31491-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31491-37:
(7*3)+(6*1)+(5*4)+(4*9)+(3*1)+(2*3)+(1*7)=99
99 % 10 = 9
So 31491-37-9 is a valid CAS Registry Number.

31491-37-9Relevant academic research and scientific papers

Synthesis of 3-fluoro-2,5-disubstituted furans through ring expansion ofgem-difluorocyclopropyl ketones

Amii, Hideki,Matsumura, Chihori,Sugiishi, Tsuyuka

, p. 3459 - 3462 (2020/05/25)

The synthesis of 3-fluoro-2,5-disubstituted furans fromgem-difluorocyclopropyl ketones was accomplished using trifluoromethanesulfonic acid (CF3SO3H) through ring expansion owing to the activation of the carbonyl group in the starting material. The present synthesis of 3-fluorofurans tolerates substrates designed for products with aromatic substituents at the C-2 and C-5 positions.

Au-catalyzed intramolecular hydroalkoxylation of gem-difluorinated alkynols

Hamel, Jean-Denys,Paquin, Jean-Fran?ois

, p. 11 - 23 (2018/10/20)

The intramolecular hydroalkoxylation of gem-difluorinated alkynols was found possible under Au catalysis, allowing for the preparation of a series of fluorinated heterocycles. The nature of the solvent was found to be especially critical in the cyclizatio

Ionic liquid, surrogate hydrogen bromide reagent for ring opening of cyclopropyl ketones

Xu, Wei,Dolbier Jr., William R.,Salazar, Jose

, p. 3535 - 3538 (2008/09/20)

(Chemical Equation Presented) Ionic liquid reagents created by addition of 1 equiv of either CF3CO2H or CF3SO3H to N-pentylpyridinium bromide exhibit excellent chemical reactivities as surrogate HBr reagents in ring-opening reactions of cyclopropyl ketones as well as of 2,2-difluorocyclopropyl ketones to form the respective 3-bromopropyl or 3-bromo-2,2-difluoropropyl ketones in good to excellent yields.

Synthesis of 3-fluoro-2,5-disubstituted furans and further derivative reactions to access fluorine-containing 3,3′-bifurans and tetrasubstituted furans

Li, Peng,Chai, Zhuo,Zhao, Gang,Zhu, Shi-Zheng

body text, p. 2547 - 2551 (2009/04/12)

2,5-Disubstituted 3-fluorofurans were synthesized in 42-99% yield via DBU-promoted cyclization reactions of electrondeficient gem- difluorohomopropargyl alcohols. Starting from these compounds, a series of fluorinated 3,3′-bifurans and tetrasubstituted fu

Selective synthesis of fluorinated furan derivatives via AgNO 3-catalyzed activation of an electronically deficient triple bond

Arimitsu, Satoru,Hammond, Gerald B.

, p. 8559 - 8561 (2008/02/12)

(Chemical Equation Presented) The transition metal-catalyzed direct activation of electron deficient triple bonds was investigated by using the combined electron withdrawing effects of two fluorine atoms to modulate the electronic density of the triple bo

A New and Concise Synthesis of 3-Fluoro-2,5-disubstituted Furans

Sham, Hing L.,Betebenner, David A.

, p. 1134 - 1135 (2007/10/02)

A highly efficient synthesis of a series of 3-fluoro-2,5-disubstituted furans by a two-step sequence is described.

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