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2-(but-3-en-1-yl)cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78707-65-0

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78707-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78707-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78707-65:
(7*7)+(6*8)+(5*7)+(4*0)+(3*7)+(2*6)+(1*5)=170
170 % 10 = 0
So 78707-65-0 is a valid CAS Registry Number.

78707-65-0Relevant academic research and scientific papers

Electrocatalytic generation of amidyl radicals for olefin hydroamidation: Use of solvent effects to enable anilide oxidation

Zhu, Lin,Xiong, Peng,Mao, Zhong-Yi,Wang, Yong-Heng,Yan, Xiaomei,Lu, Xin,Xu, Hai-Chao

, p. 2226 - 2229 (2016/02/19)

Oxidative generation of synthetically important amidyl radicals from N-H amides is an appealing and yet challenging task. Previous methods require a stoichiometric amount of a strong oxidant and/or a costly noble-metal catalyst. We report herein the first electrocatalytic method that employs ferrocene (Fc), a cheap organometallic reagent, as the redox catalyst to produce amidyl radicals from N-aryl amides. Based on this radical-generating method, an efficient intramolecular olefin hydroamidation reaction has been developed. Easy access to N-arylamidyl radicals: The first electrocatalytic method for the generation of amidyl radicals from anilides has been developed using ferrocene (Cp2Fe) as a highly reactive, yet chemoselective redox catalyst. Based on this radical-generating method, a highly chemo- and diastereoselective olefin hydroamidation reaction has been developed.

ACID CATALYZED COPE REARRANGEMENTS OF 2-ACYL-1,5-DIENES

Dauben, William G.,Chollet, Andre

, p. 1583 - 1586 (2007/10/02)

The Cope rearrangement of 1,5-dienes bearing acyl substitutents in the 2-position of the diene system is strongly accelerated by protic and Lewis acids.

A Total Synthesis of (+/-)-Eremophilenolide

Pennanen, Seppo

, p. 261 - 264 (2007/10/02)

(+/-)-Eremophilenolide was synthesized in 18percent overall yield from cyclohexanone.The A/B-ring system was prepared via butenylcyclohexenol-annulation and the 2-furanone unit via α-epoxyketone-ynamine reaction.

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