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2,3-Pentadienoic acid, 4-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65359-73-1

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65359-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65359-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65359-73:
(7*6)+(6*5)+(5*3)+(4*5)+(3*9)+(2*7)+(1*3)=151
151 % 10 = 1
So 65359-73-1 is a valid CAS Registry Number.

65359-73-1Relevant academic research and scientific papers

Synthesis of Allenyl Esters by Horner-Wadsworth-Emmons Reactions of Ketenes Mediated by Isopropylmagnesium Bromide

Sano, Shigeki,Matsumoto, Tomoya,Yano, Teppei,Toguchi, Munehisa,Nakao, Michiyasu

, p. 2135 - 2138 (2015/09/15)

The synthesis of conjugated allenyl esters (tri-substituted allenes) was achieved by magnesium(II)-mediated Horner-Wadsworth-Emmons reaction of methyl bis(2,2,2-trifluoroethyl)phosphonoacetate with disubstituted ketenes. In addition, a novel access to α-fluorinated allenyl carboxamides (tetrasubstituted allenes) is presented.

Bifunctionalized allenes. Part VIII. An efficient and varied method for the synthesis of 2-sulfonylated alka-2,3-dienoates

Ivanov, Ivaylo K.,Christov, Valerij Ch.

supporting information, p. 913 - 919 (2013/08/23)

An efficient and varied method for the synthesis of 2-sulfonylated alka-2,3-dienoates by intermediate formation of allenecarboxylates, allenyl sulfones, and propargyl sulfinates using the relatively high acidity of the hydrogen atom at the allenic C-1 ato

Enantioselective nickel-catalyzed cross-coupling reactions of trialkynylindium reagents with racemic secondary benzyl bromides

Caeiro, Jorge,Sestelo, Jose Perez,Sarandeses, Luis A.

, p. 741 - 746 (2008/12/22)

The first enantioselective sp-sp3 cross-coupling reaction between alkynyl organometals and racemic benzyl bromides is reported. The coupling is performed at room temperature by using NiBr2.diglyme and (S)-(/Pr)-Pybox as the catalytic

Iron porphyrin-catalyzed olefination of ketenes with diazoacetate for the enantioselective synthesis of allenes

Li, Chuan-Ying,Wang, Xiao-Bing,Sun, Xiu-Li,Tang, Yong,Zheng, Jun-Cheng,Xu, Zheng-Hu,Zhou, Yong-Gui,Dai, Li-Xin

, p. 1494 - 1495 (2007/10/03)

In the presence of Ph3P and catalytic Fe(TCP)Cl, ketenes could react with EDA to give allenes in high yields under neutral conditions for the first time. By employing chiral phosphine instead of PPh3, allenes could be synthesized with high enantioselectivity (93-98% ee) in good yields. Copyright

Olefination of ketenes for the enantioselective synthesis of allenes via an ylide route

Li, Chuan-Ying,Zhu, Ben-Hu,Ye, Long-Wu,Jing, Qing,Sun, Xiu-Li,Tang, Yong,Shen, Qi

, p. 8046 - 8053 (2008/02/08)

Pseudo-C2-symmetric chiral phosphorus ylide is designed and synthesized for the enantioselective preparation of allenic esters, amides, ketone, and nitrile. Up to 92% ee is achieved.

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