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96220-15-4

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96220-15-4 Usage

General Description

3-(4-Ethylphenyl)-3-oxopropanenitrile is a chemical compound with the molecular formula C11H11NO. It is a nitrile derivative containing a phenyl group with an ethyl substituent. 3-(4-Ethylphenyl)-3-oxopropanenitrile is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It is also utilized in the production of agrochemicals, dyes, and pigments. Its chemical structure and properties make it suitable for use in a wide range of applications, from industrial processes to research and development in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 96220-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,2 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96220-15:
(7*9)+(6*6)+(5*2)+(4*2)+(3*0)+(2*1)+(1*5)=124
124 % 10 = 4
So 96220-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO/c1-2-9-3-5-10(6-4-9)11(13)7-8-12/h3-6H,2,7H2,1H3

96220-15-4SDS

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 3-(4-Ethylphenyl)-3-oxopropanenitrile

1.2 Other means of identification

Product number -
Other names 3-(4-Aethyl-phenyl)-3-oxo-propionitril

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:96220-15-4 SDS

96220-15-4Downstream Products

96220-15-4Relevant articles and documents

Synthesis of benzoylacetonitriles from Pd-catalyzed carbonylation of aryl iodides and trimethylsilylacetonitrile

Park, Ahbyeol,Lee, Sunwoo

, p. 1118 - 1121 (2012)

Palladium-catalyzed carbonylation of aryl iodides and trimethylsilylacetonitrile to produce benzoylacetonitrile derivatives through a one-pot, three-component reaction is described. This preparation method provides good yields of the carbonylated products without any additional ligands. It has a broad substrate scope with a high tolerance for a variety of functional groups.

5- OR 7-AZAINDAZOLES AS BETA-LACTAMASE INHIBITORS

-

Page/Page column 41; 42, (2020/09/19)

The present invention relates to β-lactamase inhibitors having the following general formula (I): wherein R1-R4 and X1-X2 are defined in the specification, pharmaceutical composition thereof, and use thereof for the treatment of a bacterial infection, alone or in combination with β-lactam antibiotics and/or other antibiotics and/or other β-lactamase inhibitors.

Microwave synthesis of 1-aryl-1H-pyrazole-5-amines

Everson, Nikalet,Yniguez, Kenya,Loop, Lauren,Lazaro, Horacio,Belanger, Briana,Koch, Grant,Bach, Jordan,Manjunath, Aashrita,Schioldager, Ryan,Law, Jarvis,Grabenauer, Megan,Eagon, Scott

, p. 72 - 74 (2018/11/30)

A microwave-mediated synthesis of 1H-pyrazole-5-amines utilizing 1 M HCl at 150 °C was developed in order to provide products in a matter of minutes with minimal purification. Most reactions are complete in only 10 min and can be isolated via a simple filtration without the need for further purification by column chromatography or recrystallization. This method tolerates a range of functional groups and can be performed on milligram to gram scales.

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