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1-Dodecen-3-ol, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86668-28-2

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86668-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86668-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,6 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86668-28:
(7*8)+(6*6)+(5*6)+(4*6)+(3*8)+(2*2)+(1*8)=182
182 % 10 = 2
So 86668-28-2 is a valid CAS Registry Number.

86668-28-2Downstream Products

86668-28-2Relevant academic research and scientific papers

Regioselective Acetoxylation of Terminal Olefins Using a Palladium(II)–Thiadiazole Catalyst

Li, Xiaohan,Sun, Bin,Zhou, Jiadi,Jin, Can,Yu, Chuangming

, p. 2635 - 2638 (2019/04/04)

First-time use of a palladium(II)–thiadiazole catalyst in the allylic oxidation of terminal olefins to linear allylic acetates. Employing this strategy, a range of allylic esters (20 examples) were synthesized in 43 % to 80 % yield with excellent regio- and stereoselectivities.

A survey of sulfide ligands for allylic C-H oxidations of terminal olefins

Le, Chichip Q.,Kunchithapatham, Kamala,Henderson, William H.,Check, Christopher T.,Stambuli, James P.

supporting information, p. 11153 - 11157 (2013/09/02)

Perfect to a THT! Screening a diverse library of thioether ligands led to the discovery of tetrahydrothiophene (THT) as a highly reactive and selective ligand for Pd-catalyzed allylic C-H oxidation reactions (see scheme). This novel ligand system provides some of the highest reported yields for the formation of (E)-linear allylic acetates through allylic C-H activation chemistry (BQ = 1,4-benzoquinone). Copyright

Allylic oxidations of terminal olefins using a palladium thioether catalyst

Henderson, William H.,Check, Christopher T.,Proust, Nicolas,Stambuli, James P.

supporting information; experimental part, p. 824 - 827 (2010/04/06)

"Chemical equation presented" A palladium catalyst that converts terminal olefins to linear allylic acetates at lower catalyst loadings and faster reaction times than current systems is reported. This reaction can be conducted using benzoquinone as the oxidizing agent or catalytic amounts of copper and hydroquinone under one atmosphere of oxygen. Preliminary reactivity studies of π-allylpalladium complexes under our reaction conditions do not provide results similar to those obtained in the catalytic reaction, which may suggest an alternative reaction pathway. The palladium catalyst is ligated by an aryloxyalkyl aryl sulfide, which is identified as a new ligand for homogeneous catalysis.

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