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

136490-40-9

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136490-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136490-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,9 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136490-40:
(8*1)+(7*3)+(6*6)+(5*4)+(4*9)+(3*0)+(2*4)+(1*0)=129
129 % 10 = 9
So 136490-40-9 is a valid CAS Registry Number.

136490-40-9Downstream Products

136490-40-9Relevant academic research and scientific papers

A metal-free yne-addition/1,4-aryl migration/decarboxylation cascade reaction of alkynoates with Csp3-H centers

Kong, De-Long,Cheng, Liang,Wu, Hong-Ru,Li, Yang-Xiong,Wang, Dong,Liu, Li

, p. 2210 - 2217 (2016)

A metal-free cascade reaction of aryl alkynoates with five different types of radical precursors (R-H) through an yne-addition/1,4-aryl migration/decarboxylation process was reported, which allowed facile and convenient access to functionalized vinyl products with "R" and protons located at the identical carbon of the formed double bond.

Metal-Free Microwave-Assisted Decarboxylative Elimination for the Synthesis of Olefins

Wu, Shu-Wei,Liu, Jia-Li,Liu, Feng

supporting information, p. 1 - 3 (2016/01/15)

A metal-free efficient synthesis of olefins via microwave-assisted direct decarboxylative elimination of arylacetic acids is described. This reaction, using commercially available reagent PIFA as oxidant, readily provides a variety of desired products in moderate to good yields.

A transition-metal-free Heck-type reaction between alkenes and alkyl iodides enabled by light in water

Liu, Wenbo,Li, Lu,Chen, Zhengwang,Li, Chao-Jun

, p. 6170 - 6174 (2015/06/08)

A transition-metal-free coupling protocol between various alkenes and non-activated alkyl iodides has been developed by using photoenergy in water for the first time. Under UV irradiation and basic aqueous conditions, various alkenes efficiently couple with a wide range of non-activated alkyl iodides. A tentative mechanism, which involves an atom transfer radical addition process, for the coupling is proposed.

Dimeric Metal Complexes as Mediator for Radical C-C Bond-Forming Reactions

Giese, Bernd,Thoma, Gebhard

, p. 1135 - 1142 (2007/10/02)

Irradiation of dicarbonyl(η5-cyclopentadienyl)iron dimer 1 or decacarbonyldimanganese (2) in the presence of alkyl halides leads to C-centered radicals which can be trapped by alkenes and yields saturated and/or unsaturated addition products.Carbon radicals are generated via halogen abstraction by the initially formed metal-centered radicals resulting from homolysis of the metal-metal bond of dimeric mediators 1 and 2.No reaction occurs using octacarbonyl dicobalt (3).

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