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4-methyl-3-phenyl-2-cyclopentenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26131-96-4

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26131-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26131-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26131-96:
(7*2)+(6*6)+(5*1)+(4*3)+(3*1)+(2*9)+(1*6)=94
94 % 10 = 4
So 26131-96-4 is a valid CAS Registry Number.

26131-96-4Relevant academic research and scientific papers

Regio- and stereoselective synthesis of cyclopentenones: Intermolecular Pseudo-Pauson-Khand cyclization

Barluenga, Jose,Alvarez-Fernandez, Ana,Suarez-Sobrino, Angel L.,Tomas, Miguel

supporting information; experimental part, p. 183 - 186 (2012/03/26)

Doing the two step: A very simple two-step access to polysubstituted cyclopentenones from terminal alkynes, [M(CO)6], and bromoalkenes is described. This protocol is an alternative to the intermolecular Pauson-Khand reaction, and can be used wi

Rearrangement of 1-(1-alkynyl)cyclopropanols to 2-cyclopentenones via their hexacarbonyldicobalt complexes. A new use of alkyne-CO2(CO)6 complexes in organic synthesis

Iwasawa, Nobuharu,Matsuo, Takeshi,Iwamoto, Mari,Ikeno, Taketo

, p. 3903 - 3914 (2007/10/03)

A novel rearrangement of 1-(1-alkynyl)cyclopropanols to 2-cyclopenten- 1-ones proceeded on complexation of their alkynyl part with octacarbonyldicobalt (Co2(CO8)). 1-(1-Alkynyl)cyclopropanols with a wide range of substituents on thei

A Conformationally Controlled Regioselective of 2-Substituted 1-Alkynylcyclopropanols to 2-Cyclopenten-1-ones via Hexacarbonyldicobalt Complex

Iwasawa, Nobuharu,Iwamoto, Mari

, p. 1257 - 1260 (2007/10/02)

The rearrangement of hexacarbonyldicobalt-complexed 2-substituted 1-alkynylcyclopropanol derivatives is conformationally controlled to give 3- or 5-substituted 2-cyclopentanones regioselectively.In the cases of the reactions of 2-monosubstituted 1-alkynyl

DIASTEREOSELECTION IN RHODIUM-MEDIATED INTRAMOLECULAR C-H INSERTION: PREPARATION OF A TRANS-3,4 DIALKYL CYCLOPENTANE

Taber, Douglass F.,Ruckle, Robert E.

, p. 3059 - 3062 (2007/10/02)

Transition state analysis suggests that substantial 1,2 asymmetric induction could be observed in the course of rhodium-mediated intramolecular C-H insertion.This analysis succesfully predicts predominant formation of the trans 3,4-dialkyl cyclopentane wh

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