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2-methoxy-5-(trifluoromethyl)nicotinonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124432-68-4

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124432-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124432-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,3 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124432-68:
(8*1)+(7*2)+(6*4)+(5*4)+(4*3)+(3*2)+(2*6)+(1*8)=104
104 % 10 = 4
So 124432-68-4 is a valid CAS Registry Number.

124432-68-4Downstream Products

124432-68-4Relevant academic research and scientific papers

A room temperature cyanation of (hetero)aromatic chlorides by an air stable nickel(II) XantPhos precatalyst and Zn(CN)2

Beattie, D. Dawson,Schareina, Thomas,Beller, Matthias

supporting information, p. 4291 - 4294 (2017/07/10)

A methodology for the synthesis of (hetero)aromatic nitriles from aryl chlorides at room temperature has been developed. This methodology uses an air and moisture stable nickel(ii) XantPhos precatalyst and Zn(CN)2 as the cyanide (CN-) source.

N-(PYRIDIN-3-YL)-2-PHENYLBUTANAMIDES AS ANDROGEN RECEPTOR MODULATORS

-

Page/Page column 42, (2010/11/08)

Compounds of structural formula (I) are modulators of the androgen receptor (AR) in a tissue selective manner. These compounds are useful in the enhancement of weakened muscle tone and the treatment of conditions caused by androgen deficiency or which can

N-cyanomethyl-2-pyridinone insecticides

-

, (2008/06/13)

Substituted N-cyanomethyl-2-pyridinones were prepared by the reaction of alkali metal substituted-2-pyridinates with monohaloacetonitriles and found to possess insecticidal properties. The alkali metal substituted-2-pyridinates can be preformed or prepared from the corresponding 2-halopyridines or 2-pyridinols in the reaction medium. N-cyanomethyl-3-fluoro-5-(trifluoromethyl)-2-pyridinone, for example, was prepared from 2,3-difluoro-5-(trifluoromethyl)pyridine and found to control aster leafhoppers both on contact and systemically.

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