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4-(4-methyl-2-nitrophenyl)pyridine is an organic compound characterized by its molecular formula C12H10N2O2. 4-(4-methyl-2-nitrophenyl)pyridine features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a 4-methyl-2-nitrophenyl group attached to it. The 4-methyl-2-nitrophenyl group consists of a benzene ring with a methyl group at the 4-position and a nitro group at the 2-position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that handling and disposal of 4-(4-methyl-2-nitrophenyl)pyridine should be done with care, as it may have hazardous properties.

4373-69-7

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4373-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4373-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4373-69:
(6*4)+(5*3)+(4*7)+(3*3)+(2*6)+(1*9)=97
97 % 10 = 7
So 4373-69-7 is a valid CAS Registry Number.

4373-69-7Relevant academic research and scientific papers

COMPOUNDS USEFUL FOR INHIBITING CHK1

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Page/Page column 44, (2008/06/13)

Substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as ther-apeutic agents, for example, in treating cancer and oth

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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