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(E)-1-methoxy-4-(non-2-en-1-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106470-35-3

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106470-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106470-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,7 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106470-35:
(8*1)+(7*0)+(6*6)+(5*4)+(4*7)+(3*0)+(2*3)+(1*5)=103
103 % 10 = 3
So 106470-35-3 is a valid CAS Registry Number.

106470-35-3Downstream Products

106470-35-3Relevant academic research and scientific papers

Merging photoredox and nickel catalysis: Decarboxylative cross-coupling of carboxylic acids with vinyl halides

Noble, Adam,McCarver, Stefan J.,Macmillan, David W. C.

, p. 624 - 627 (2015)

Decarboxylative cross-coupling of alkyl carboxylic acids with vinyl halides has been accomplished through the synergistic merger of photoredox and nickel catalysis. This new methodology has been successfully applied to a variety of α-oxy and α-amino acids, as well as simple hydrocarbon-substituted acids. Diverse vinyl iodides and bromides give rise to vinylation products in high efficiency under mild, operationally simple reaction conditions.

Cross-Coupling Reactions of Alkenyl Halides with 4-Benzyl-1,4- Dihydropyridines Associated with E to Z Isomerization under Nickel and Photoredox Catalysis

Nakajima, Kazunari,Guo, Xifeng,Nishibayashi, Yoshiaki

supporting information, p. 3653 - 3657 (2018/11/10)

Cross-coupling reactions of alkenyl halides with 4-alkyl-1,4-dihydropyridines as alkylation reagents have been achieved by combination of nickel and photoredox catalysts. Alkenyl halides bearing alkyl and aryl substituents are available. Particularly, in

Cross-coupling reaction of allylic and benzylic carbonates with organo[2-(hydroxymethyl)phenyl]dimethylsilanes

Nakao, Yoshiaki,Ebata, Shiro,Chen, Jinshui,Imanaka, Hidekazu,Hiyama, Tamejiro

, p. 606 - 607 (2008/02/07)

The title reaction is found to proceed in the presence of a palladium catalyst and in the absence of any activator. Various functional groups are tolerated to give a diverse range of 1,4-diene and diarylmethane products, which are ubiquitous units of natural products and pharmaceuticals. Copyright

A Total Synthesis of the Methyl Ester of the 9,11-Dithia Analogue of 13,14-Dehydro-PGH2

Ghosh, Soumitra S.,Martin, John C.,Fried, Josef

, p. 862 - 876 (2007/10/02)

A total synthesis of the disulfide analogue 2 of 13,14-dehydro-PGH2 methyl ester is described.A key intermediate is the mesylate of the 3-phenyl-2,4-dithiabicyclooctane derivative 37b, which undergoes alkynylation via an episulfonium intermediate t

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