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(S,S,S)-2,3-dimethyl-5-(2-propen-2-yl)-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160961-89-7

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160961-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160961-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,9,6 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 160961-89:
(8*1)+(7*6)+(6*0)+(5*9)+(4*6)+(3*1)+(2*8)+(1*9)=147
147 % 10 = 7
So 160961-89-7 is a valid CAS Registry Number.

160961-89-7Relevant academic research and scientific papers

Synthesis of the insect pheromone (2S,3S,7RS)-diprionyl acetate by diastereoselective protonation

Ebert, Sophia,Krause, Norbert

, p. 3831 - 3835 (2001)

The insect pheromone (2S,3S,7RS)-diprionyl acetate (1) was prepared from (S,S)-2,3-dimethylcyclohexanone (2), which in turn was obtained by the 1,4-addition of lithium dimethylcuprate to (S)-(+)-carvone (3) and diastereoselective protonation of the result

The First Synthesis of (–)-Agelasine F; an Antimycobacterial Natural Product Found in Marine Sponges in the Agelas Genus

Gundersen, Lise-Lotte,Paulsen, Britt

, (2020/04/16)

(–)-Agelasine F (also known as ageline A) is a diterpene-adenine hybrid natural product isolated from marine sponges (Agelas species) and this compound is known to display cytotoxic activity against a variety of cancer cell lines as well as microorganisms. We herein report the first total synthesis of (–)-agelasine F. The commercially available and inexpensive monoterpenoid (S)-carvone was found to be a highly suitable starting material for the construction of the terpenoid part of the desired agelasine and controlling the stereochemistry of the target compound. Two alternative strategies from (S)-carvone were evaluated. Key-intermediates in the (–)-agelasine F synthesis are believed also to be valuable starting materials for total syntheses of other bioactive marine sponge metabolites. The synthetic route to (–)-agelasine F described herein is more efficient than previously published syntheses of racemic or ent-agelasine F.

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