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phenyl(3-phenyl-1H-indol-1-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99872-44-3

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99872-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99872-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,7 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99872-44:
(7*9)+(6*9)+(5*8)+(4*7)+(3*2)+(2*4)+(1*4)=203
203 % 10 = 3
So 99872-44-3 is a valid CAS Registry Number.

99872-44-3Downstream Products

99872-44-3Relevant academic research and scientific papers

Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles

Yuan, Hairui,Guo, Lirong,Liu, Fengting,Miao, Zechen,Feng, Lei,Gao, Hongyin

, p. 3906 - 3912 (2019/04/25)

Herein, we developed a copper-catalyzed O-vinylation of arylhydroxylamine using vinyliodonium salts as vinylation reagents to generate a transient O-vinyl-N-arylhydroxylamine that rapidly undergoes a [3,3]-sigmatropic rearrangement and subsequent cyclizat

HFIP-promoted Bischler indole synthesis under microwave irradiation

Yao, Guangkai,Zhang, Zhi-Xiang,Zhang, Cheng-Bei,Xu, Han-Hong,Tang, Ri-Yuan

, (2019/01/03)

1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP) was found to be effective for the Bischler indole synthesis under microwave irradiation in the absence of a metal catalyst. Under the catalysis of HFIP, a wide range of α-amino arylacetones were successfully transf

Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylanilides: Synthesis of 3-Substituted Indoles by 1,2-Carbon Migration

Watanabe, Takuma,Mutoh, Yuichiro,Saito, Shinichi

supporting information, p. 7749 - 7752 (2017/06/21)

We developed ruthenium-catalyzed cycloisomerization of alkynylanilides that gave 3-substituted indoles in high yields. The reaction proceeded via the disubstituted vinylidene ruthenium complex that was formed by the 1,2-carbon migration.

Aerobic palladium(II)-catalyzed dehydrogenation of cyclohexene-1-carbonyl indole amides: An indole-directed aromatization

Kandukuri, Sandeep R.,Oestreich, Martin

, p. 8750 - 8755 (2012/11/07)

A palladium(II)-catalyzed oxidative dehydrogenation of cyclohexene-1- carbonyl indole amides yielding the corresponding benzoylindoles is reported. The new aromatization is also applied to functionalized indoles such as tryptamine and tryptophan. The tethered indole is likely acting as a directing group for allylic C-H bond activation, and there is evidence for a mechanism proceeding through 1,3-diene formation followed by aromatization.

Process for producing indoline compounds and intermediates for the production of the same

-

, (2008/06/13)

This invention concerns a method for the production of a 3-arylindoline compound represented by the general formula STR1

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