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1440429-92-4

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1440429-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440429-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,4,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1440429-92:
(9*1)+(8*4)+(7*4)+(6*0)+(5*4)+(4*2)+(3*9)+(2*9)+(1*2)=144
144 % 10 = 4
So 1440429-92-4 is a valid CAS Registry Number.

1440429-92-4Relevant academic research and scientific papers

A facile method for the synthesis of dihydroquinoline-Azide from the Lewis acid-catalyzed reaction of alkylidenecyclopropanes with TMSN3

Chen, Mintao,Wei, Yin,Shi, Min

, p. 9990 - 9993 (2019)

A facile synthetic method for the formation of dihydroquinoline-Azide from alkylidenecyclopropanes and TMSN3 under the catalysis of a Lewis acid has been developed, and a number of azide-containing compounds can be instantly accessed in moderate to good yields. A click reaction with these azido compounds was also realized along with a mechanistic investigation.

Palladium-catalyzed oxidative cyclization of aniline-tethered alkylidenecyclopropanes with O2: a facile protocol to selectively synthesize 2- and 3-vinylindoles

Cao, Bo,Simaan, Marwan,Marek, Ilan,Wei, Yin,Shi, Min

, p. 216 - 219 (2016/12/27)

A novel palladium-catalyzed oxidative cyclization of aniline-tethered alkylidenecyclopropanes using molecular oxygen as the terminal oxidant through β-carbon elimination of aminopalladation intermediates is disclosed. The reaction opens up an effective way to obtain a series of 2- and 3-vinylindoles which are important synthetic intermediates in many natural indole derivatives.

Palladium-catalyzed cascade cyclization of allylamine-tethered alkylidenecyclopropanes: Facile access to iodine/difluoromethylene- and perfluoroalkyl-containing 1-benzazepine scaffolds

Yu, Liu-Zhu,Zhu, Zi-Zhong,Hu, Xu-Bo,Tang, Xiang-Ying,Shi, Min

supporting information, p. 6581 - 6584 (2016/06/01)

The unprecedented palladium-catalyzed cascade cyclization of allylamine-tethered alkylidenecyclopropanes with an ethyl difluoroiodoacetate or perfluoroalkylated reagent is developed, providing facile access to a variety of synthetically and medicinally valuable iodine/difluoromethylene- and perfluoroalkyl-containing 1-benzazepine frameworks. These reactions exhibited good yields and functional group tolerance via a radical mechanism.

Copper(I)-Catalyzed Intramolecular Trifluoromethylation of Methylenecyclopropanes

Zhu, Zi-Zhong,Chen, Kai,Yu, Liu-Zhu,Tang, Xiang-Ying,Shi, Min

supporting information, p. 5994 - 5997 (2016/01/09)

Copper(I)-catalyzed intramolecular trifluoromethylation of methylenecyclopropanes has been developed to produce a variety of CF3-substituted dihydronaphthalenes in moderate to good yields, relying on the construction of C(sp2)-CFsub

Thermal induced intramolecular [2 + 2] cycloaddition of allene-ACPs

Chen, Kai,Sun, Run,Xu, Qin,Wei, Yin,Shi, Min

supporting information, p. 3949 - 3953 (2013/07/05)

A facile synthetic method for preparation of bicyclo[4.2.0] nitrogen heterocycles has been developed via a thermal induced intramolecular [2 + 2] cycloaddition reaction of allene-ACPs. The DFT calculations indicate that this intramolecular cycloaddition proceeds in a concerted manner and a strained small ring is essential. The Royal Society of Chemistry 2013.

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