13288-86-3 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
Ethyl 3-(cyanomethyl)-benzoate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new compounds with therapeutic and pesticidal properties.
Used in Perfumery and Flavoring Industry:
Ethyl 3-(cyanomethyl)-benzoate is used as a component in the manufacturing of perfumes and flavorings due to its distinctive fruity scent, enhancing the fragrance and taste profiles of various products.
Used in Insecticide Production:
Ethyl 3-(cyanomethyl)-benzoate is used as an ingredient in the production of insect repellents, capitalizing on its potential as an insecticide to protect against unwanted pests.
Safety Precautions:
It is important to handle ethyl 3-(cyanomethyl)-benzoate with care, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes. Proper safety measures should be taken during its use and storage to minimize health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 13288-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,8 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13288-86:
(7*1)+(6*3)+(5*2)+(4*8)+(3*8)+(2*8)+(1*6)=113
113 % 10 = 3
So 13288-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO2/c1-2-14-11(13)10-5-3-4-9(8-10)6-7-12/h3-5,8H,2,6H2,1H3
13288-86-3Relevant academic research and scientific papers
Pd-catalyzed α-arylation of nitriles and esters and γ-arylation of unsaturated nitriles with TMPZnCl?LiCl
Duez, Stephanie,Bernhardt, Sebastian,Heppekausen, Johannes,Fleming, Fraser F.,Knochel, Paul
, p. 1690 - 1693 (2011/05/06)
Using TMPZnCl?LiCl as a kinetically highly active base, nitriles and esters undergo a Pd-catalyzed α-arylation under mild conditions. Remarkably, in the case of α,β- or β,γ-unsaturated nitriles, a regioselective γ-arylation or a γ-alkenylation is observed.
