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1114-73-4

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1114-73-4 Usage

General Description

2-Cyanononanoic acid ethyl ester, also known as ethyl 2-cyano-9-oxononanoate, is an organic compound with the chemical formula C11H19NO3. It is a ester derivative of 2-cyanononanoic acid and is commonly used in organic synthesis and as a chemical intermediate in the production of pharmaceuticals and other organic compounds. It is a colorless liquid with a fruity odor, and it is soluble in most organic solvents. 2-Cyanononanoic acid ethyl ester is considered to be a potentially hazardous substance and should be handled with care, following proper safety precautions and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 1114-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1114-73:
(6*1)+(5*1)+(4*1)+(3*4)+(2*7)+(1*3)=44
44 % 10 = 4
So 1114-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO2/c1-3-5-6-7-8-9-11(10-13)12(14)15-4-2/h11H,3-9H2,1-2H3

1114-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyanononanoate

1.2 Other means of identification

Product number -
Other names 2-Cyan-nonansaeure-aethylester

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:1114-73-4 SDS

1114-73-4Downstream Products

1114-73-4Relevant articles and documents

One-pot multistep cascade reactions over multifunctional nanocomposites with pd nanoparticles supported on amine-modified mesoporous silica

Li, Ping,Liu, Hua,Yu, Yu,Cao, Chang-Yan,Song, Wei-Guo

, p. 2459 - 2465 (2013)

Two kinds of multifunctional nanocomposites, SBA-15-NH2/Pd-p and SBA-15-NH2/Pd-f, with platelet-like and fiber-like morphologies, respectively, were fabricated by immobilizing Pd NPs onto amine-functionalized SBA-15. Some of the amino groups acted as anchoring sites for Pd NPs, whilst the remaining groups acted as Bronsted basic sites. As a result, the composites served as excellent multifunctional heterogeneous catalysts for one-pot multistep cascade reaction sequences. Moreover,when diffusion was the rate-determine step, SBA-15-NH2/Pd-p, with small mesopores, was superior to the fiber-like control sample, owing to its short diffusion length, a lower possibility of pore clogging, and better mass transportation for the reaction species during the catalysis.

Towards organo-click reactions: Development of pharmaceutical ingredients by using direct organocatalytic bio-mimetic reductions

Ramachary, Dhevalapally B.,Reddy, G. Babul

, p. 4463 - 4468 (2008/09/19)

Economic and environmentally friendly bio-mimetic one-pot three and four-component Knoevenagel-hydrogenation (K-H), five-component Knoevenagel-hydrogenation-alkylation (K-H-A) and six-component Knoevenagel-hydrogenation-alkylation-Huisgen cycloaddition (K-H-A-HC) reactions of aldehydes, CH-acids, o-phenylenediamine, alkyl halides and azides using proline, proline-metal carbonate and proline-metal carbonate-Cu I-catalysis, respectively have been developed. Many of K-H and K-H-A compounds have direct application in pharmaceutical chemistry. The Royal Society of Chemistry.

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