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Pyridine, 3-(4-chloro-2-nitrophenyl)-, also known as 3-(4-Chloro-2-nitrophenyl)pyridine, is an organic compound with the chemical formula C11H7ClN2O2. It is a derivative of pyridine, a heterocyclic aromatic compound with a nitrogen atom in the ring structure. This particular compound features a 4-chloro-2-nitrophenyl group attached to the 3-position of the pyridine ring. The presence of the chlorine and nitro groups imparts unique chemical properties to the molecule, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is essential to handle Pyridine, 3-(4-chloro-2-nitrophenyl)- with care, following proper safety protocols and guidelines.

4423-07-8

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4423-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4423-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4423-07:
(6*4)+(5*4)+(4*2)+(3*3)+(2*0)+(1*7)=68
68 % 10 = 8
So 4423-07-8 is a valid CAS Registry Number.

4423-07-8Relevant academic research and scientific papers

Synthesis of nitrogen heterocycles by the ring opening of pyridinium salts

Kearney, Aaron M.,Vanderwal, Christopher D.

, p. 7803 - 7806 (2007/10/03)

(Chemical Equation Presented) The century-old ring-opening reaction of pyridinium salts with tethered nucleophiles has been harnessed for a synthesis of substituted indoles and related nitrogen heterocyles. Extension of this method could lead to oxygen- and sulfur-containing heterocycles and carbocycles, as well as to applications in natural product synthesis and medicinal chemistry.

Synthesis and antiarrhythmic activity of disubstituted phenylpyridine derivative

Shigyo,Sato,Shibuya,Takahashi,Yamaguchi,Sonoki,Ohta

, p. 1573 - 1582 (2007/10/02)

A series of disubstituted phenylpyridine derivatives was synthesized and their antiarrhythmic effects against chloroform-induced ventricular arrhythmias in mice were examined. Among them, 2- and 3-[2-(3- aminobutyramido)-4-(2,2,2-trifluoroethoxy)phenyl]pyridines (23h, 24h) and 3- [2-(3-aminobutyramido)-4-ethoxyphenyl]pyridine (24i) showed potent antiarrhythmic activity. They had approximately twice the potency of mexiletine (III). Compound 24i was selected from this series as a candidate for further development; it was found to have a class I B electrophysiological character and to show a slow kinetic rate-dependent block (RDB) of the sodium channel in cardiac muscle.

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