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2-Cyclopenten-1-one, 4,4-dimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26029-32-3

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26029-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26029-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,2 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26029-32:
(7*2)+(6*6)+(5*0)+(4*2)+(3*9)+(2*3)+(1*2)=93
93 % 10 = 3
So 26029-32-3 is a valid CAS Registry Number.

26029-32-3Downstream Products

26029-32-3Relevant academic research and scientific papers

Palladium-catalyzed intramolecular oxidative heck cyclization and its application toward a synthesis of (±)-β-cuparenone derivatives supported by computational studies

Ray, Devalina,Nasima, Yasmin,Sajal, Mal K.,Ray, Priyanka,Urinda, Sharmistha,Anoop, Anakuthil,Ray, Jayanta K.

, p. 1261 - 1269 (2013)

A novel and efficient intramolecular oxidative cyclization of substituted homoallylic alcohols to form cyclic keto compounds under palladium-catalyzed conditions is described. The reaction has practical applications in the synthesis of sesquiterpenes. The

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

Iwasawa, Nobuharu,Iwamoto, Mari

, p. 1257 - 1260 (1993)

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

Novel synthetic approach toward (±)-β-cuparenone via palladium-catalyzed tandem Heck cyclization of 1-bromo-5-methyl-1-aryl-hexa-1,5- dien-3-ol derivatives

Ray, Devalina,Ray, Jayanta K.

, p. 191 - 194 (2007/10/03)

(Chemical Equation Presented) A novel and convenient synthetic route toward (±)-β-cuparenone and many other sesquiterpene natural product precursors has been developed via palladium-catalyzed tandem Heck cyclization of 1-bromo-5-methyl-1-aryl-hexa-1,5-die

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

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