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1H-Indole, 3-(1,3-diphenyl-2-propenyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881304-41-2

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881304-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881304-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,3,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 881304-41:
(8*8)+(7*8)+(6*1)+(5*3)+(4*0)+(3*4)+(2*4)+(1*1)=162
162 % 10 = 2
So 881304-41-2 is a valid CAS Registry Number.

881304-41-2Downstream Products

881304-41-2Relevant academic research and scientific papers

Synthesis, Characterization and Catalytic Application of Starch Supported Cuprous Iodide Nanoparticles

Mallick, Sadhucharan,Mukhi, Priyabrata,Kumari, Poonam,Mahato, Kumari Reshmi,Verma, Suryadev Kumar,Das, Debjit

, p. 3501 - 3507 (2019)

Abstract: The starch supported cuprous iodide nanoparticles (CuI-NPs@Starch) were synthesized in aqueous medium and characterized by transmission electron microscopy, scanning electron microscopy, X-ray powder diffraction, energy-dispersive X-ray spectros

Dehydration in water: frustrated Lewis pairs directly catalyzed allylization of electron-rich arenes and allyl alcohols

Dong, Yu,He, Shuai,Shi, Zhi-Chuan,Wang, Ji-Yu,Yang, Jian,Zhan, Xiao-Yu,Zhang, Hua,Zhang, Xiao-Mei

, p. 16942 - 16948 (2020/05/18)

A frustrated Lewis pair (FLP)-catalyzed allylation of allyl alcohols with electron-rich arenes has been developed. Interestingly, in this reaction, the electron-rich arenes and allyl alcohols are dehydrated in water. What's more, water was the sole byproduct of the reaction. In this protocol, various allyl alcohols can be converted into allyl cations and attacked by the electron-rich arenes to form aryl cation intermediates. Finally, the aryl cation intermediates are deprotonated to give the 1,3-diarylpropenes. In this protocol, indole allyl alcohols can undergo a bimolecular ring closure reaction, and structurally diverse tetrahydroindolo[3,2-b]carbazoles could be smoothly obtained. The reaction is not sensitive to oxygen and has been performed on a gram-scale.

Direct benzylation and allylic alkylation in high-temperature water without added catalysts

Hirashita, Tsunehisa,Kuwahara, Sho,Okochi, Sota,Tsuji, Makoto,Araki, Shuki

experimental part, p. 1847 - 1851 (2010/09/07)

In high-temperature water a series of benzyl and allylic alcohols reacted with 1,3-dicarbonyl compounds and activated aromatic compounds to give the alkylated products without added catalysts.

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