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2-Tridecanol, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41015-28-5

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41015-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41015-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41015-28:
(7*4)+(6*1)+(5*0)+(4*1)+(3*5)+(2*2)+(1*8)=65
65 % 10 = 5
So 41015-28-5 is a valid CAS Registry Number.

41015-28-5Relevant academic research and scientific papers

Stabilization of long-chain intermediates in solution. octyl radicals and cations

Teodorovi?, Aleksandar V.,Badjuk, Dalibor M.,Stevanovi?, Nenad,Pavlovi?, Radoslav Z.

, p. 19 - 24 (2013/06/26)

The rearrangements of 1-octyl, 1-decyl and 1-tridecyl intermediates obtained from thermal lead(IV) acetate (LTA) decarboxylation of nonanoic, undecanoic and tetradecanoic acid were investigated experimentally through analysis and distribution of the products. The relationships between 1,5-, 1,6- and possibly existing 1,7-homolytic hydrogen transfer in 1-octyl-radical, as well as successive 1,2-hydride shift in corresponding cation have been computed via Monte-Carlo method. Taking into account that ratios of 1,5-/1,6-homolytic rearrangements in 1-octyl- and 1-tridecyl radical are approximately the same, the simulation shows very low involvement of 1,7-hydrogen rearrangement (1,5-/1,6-/1,7-hydrogen rearrangement = 85:31:1) in 1-octyl radical.

Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi

Ferrarini, Renan S.,Comasseto, Joao V.,Dos Santos, Alcindo A.

experimental part, p. 2043 - 2047 (2010/03/04)

The components of the pheromone blend of Mayetiola destructor, Drosophila mulleri, and Contarinia pisi were synthesized in high enantiomeric excess (99% ee) from a common enantiopure dianion prepared from an enantiopure hydroxytelluride.

Enantioselective Synthesis of (S)-(+)-2-Tridecanol Acetate, an Aggregation Pheromone Component of Drosophila mulleri

Enders, Dieter,Plant, Andrew

, p. 1241 - 1243 (2007/10/02)

The enantioselective synthesis of (S)-(+)-2-tridecanol acetate (ee = 93.5percent), an aggregation pheromone of Drosophila mulleri, is described.Key steps are the α-alkylation of the propiophenone SAMP-hydrazone (S)-2 (de 96percent) and the Baeyer-Villiger reaction of the ketone (S)-4.Key Words: (S)-(+)-2-Tridecanol acetate / SAMP-hydrazone / Baeyer-Villiger reaction / Pheromone, aggregation / Drosophila mulleri

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