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2-(3-phenylprop-2-en-1-ylidene)-2,3-dihydro-1H-indene-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13895-03-9

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13895-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13895-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13895-03:
(7*1)+(6*3)+(5*8)+(4*9)+(3*5)+(2*0)+(1*3)=119
119 % 10 = 9
So 13895-03-9 is a valid CAS Registry Number.

13895-03-9Downstream Products

13895-03-9Relevant academic research and scientific papers

Utilizing Vinylcyclopropane Reactivity: Palladium-Catalyzed Asymmetric [5+2] Dipolar Cycloadditions

Lan, Yu,Li, Miao-Miao,Lu, Liang-Qiu,Qu, Bao-Le,Xiao, Wen-Jing,Xiao, Yu-Qing,Xiong, Qin

, p. 17429 - 17434 (2020)

Vinylcyclopropanes (VCPs) are commonly used in transition-metal-catalyzed cycloadditions, and the utilization of their recently realized reactivities to construct new cyclic architectures is of great significance in modern synthetic chemistry. Herein, a p

Diversity-Oriented Synthesis of Spirocyclohexene Indane-1,3-diones and Coumarin-Fused Cyclopentanes via an Organobase-Controlled Cascade Reaction

Wang, Min,Tseng, Ping-Yao,Chi, Woei-Jye,Suresh, Sundaram,Edukondalu, Athukuri,Chen, Yi-Ru,Lin, Wenwei

supporting information, p. 3407 - 3415 (2020/07/16)

An organobase-controlled, divergent cascade reaction to construct spirocyclohexene indane-1,3-diones and coumarin-fused cyclopentanes is reported. The cascade reaction is triggered by the 1,6-addition of 3-homoacylcoumarins to the indanedione-derived acce

Organophosphine-catalyzed intramolecular hydroacylation of activated alkynes

Mondal, Atanu,Hazra, Raju,Grover, Jagdeep,Raghu, Moluguri,Ramasastry

, p. 2748 - 2753 (2018/04/14)

We present the details of an organophosphine-catalyzed Morita-Baylis-Hillman-type reaction of activated alkynes. The outcome is an intramolecular hydroacylation of α,β-ynones leading to the formation of 1,3-cyclopenta-, cyclohepta-, and cyclooctadione-fused arenes and heteroarenes. In addition, during the course of the investigation, a phosphine-catalyzed intramolecular aldol reaction of keto-ynones via δ′[C(sp3)-H]-functionalization was discovered, and a new annulation event comprising of a ω′[C(sp3)-H]-functionalization of α,β-ynones was also uncovered. The mechanisms governing these processes have been thoroughly elucidated.

Easy entry to donor/acceptor butadiene dyes through a MW-assisted InCl3-catalyzed coupling of propargylic alcohols with indan-1,3-dione in water

Francos, Javier,Borge, Javier,Díez, Josefina,García-Garrido, Sergio E.,Cadierno, Victorio

, p. 10 - 14 (2015/02/19)

In this contribution, the high-yield preparation and optical properties of some donor-acceptor butadiene dyes, generated by coupling of different 1,1-diaryl-2-propyn-1-ols with indan-1,3-dione, are presented. The reactions, which involve the initial Meyer

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