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13288-86-3

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13288-86-3 Usage

General Description

Ethyl 3-(cyanomethyl)-benzoate is an organic compound with the chemical formula C11H11NO2. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. This chemical is a clear liquid with a fruity odor and is often used in the manufacturing of perfumes and flavorings. Ethyl 3-(cyanomethyl)-benzoate is also known for its potential as an insecticide and is used in the production of insect repellents. It is important to handle this chemical with care as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

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

13288-86-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(cyanomethyl)benzoate

1.2 Other means of identification

Product number -
Other names 3-Cyanomethylbenzoesaeureaethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13288-86-3 SDS

13288-86-3Relevant articles and documents

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.

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