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2-(2-FLUOROBENZYL)MALONONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

338965-16-5

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338965-16-5 Usage

Malononitrile derivative

2-(2-fluorobenzyl)malononitrile is a derivative of malononitrile, meaning it is a compound that has been modified from the parent compound malononitrile.

Fluorobenzyl group

2-(2-fluorobenzyl)malononitrile has a fluorobenzyl group attached to one of its carbon atoms, which gives it unique properties and reactivity.

Building block for more complex molecules

2-(2-fluorobenzyl)malononitrile is commonly used in the synthesis of pharmaceuticals and agrochemicals as a building block for more complex molecules.

Precursor in the production of various polymers and organic compounds

2-(2-fluorobenzyl)malononitrile is also used as a precursor in the production of various polymers and other organic compounds.

Potential as a fluorescent probe

2-(2-fluorobenzyl)malonitrile has been studied for its potential as a fluorescent probe for sensing and imaging applications.

Of interest to researchers

Due to its versatile and useful properties, 2-(2-fluorobenzyl)malononitrile is of interest to researchers in various fields of chemistry and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 338965-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,9,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 338965-16:
(8*3)+(7*3)+(6*8)+(5*9)+(4*6)+(3*5)+(2*1)+(1*6)=185
185 % 10 = 5
So 338965-16-5 is a valid CAS Registry Number.

338965-16-5Relevant academic research and scientific papers

The synthesis of some derivatives based on the 4-Benzyl-1H-Pyrazole-3,5- Diamine core

Jedinak, Lukas,Krystof, Vladimir,Cankara, Petr

, p. 371 - 383 (2011/04/15)

The three-step synthesis of 4-benzyl-1H-pyrazole-3,5-diamines 2 from commercially available aldehydes 3 is given. The Knoevenagel condensation was utilized to assemble the initial carbon framework, resulting in the benzylidenemalononitriles 4 which were d

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