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2,5-bis(3-methoxyphenyl)furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1145987-34-3

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1145987-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1145987-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,5,9,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1145987-34:
(9*1)+(8*1)+(7*4)+(6*5)+(5*9)+(4*8)+(3*7)+(2*3)+(1*4)=183
183 % 10 = 3
So 1145987-34-3 is a valid CAS Registry Number.

1145987-34-3Downstream Products

1145987-34-3Relevant academic research and scientific papers

Rapid pseudo five-component synthesis of intensively blue luminescent 2,5-di(hetero)arylfurans via a Sonogashira-Glaser cyclization sequence

Klukas, Fabian,Grunwald, Alexander,Menschel, Franziska,Mueller, Thomas J. J.

, p. 672 - 679 (2014/04/17)

2,5-Di(hetero)arylfurans are readily accessible in a pseudo five-component reaction via a Sonogashira-Glaser coupling sequence followed by a superbase-mediated (KOH/DMSO) cyclization in a consecutive one-pot fashion. Besides the straightforward synthesis of natural products and biologically active molecules all representatives are particularly interesting due to their bright blue luminescence with remarkably high quantum yields. The electronic structure of the title compounds is additionally studied with DFT computations.

Mono- and biscouplings using triarylbismuths for the atom-efficient arylations of functionalized furans under palladium catalysis

Rao, Maddali L. N.,Awasthi, Dheeraj K.,Talode, Jalindar B.

supporting information; experimental part, p. 1907 - 1912 (2012/09/22)

Palladium-catalyzed cross-coupling reactions of functionalized bromofurans with triarylbismuths have been described for the atom-economic synthesis of functionalized arylfuran systems. The coupling reactions using triarylbismuths with various 2-bromofurans and 2,5-dibromofuran underwent smoothly to afford the corresponding 2-arylfurans and 2,5-diarylfurans in high yields in a short reaction time (one hour). Georg Thieme Verlag Stuttgart · New York.

Sequential synthesis of furans from alkynes: Successive ruthenium(II)- and copper(II)-catalyzed processes

Zhang, Min,Jiang, Huan-Feng,Neumann, Helfried,Beller, Matthias,Dixneuf, Pierre H.

supporting information; experimental part, p. 1681 - 1684 (2009/06/30)

(Chemical Equation Presented) Step in time: 2,5-Disubstituted furans can be prepared from terminal alkynes in one pot using two successive catalytic reactions (see scheme; p-TSA=para-toluene-sulfonic acid). First, a 1,3-dienyl alkyl ether is produced by t

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