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N-(5-methylpyridin-2-yl)benzimidamide is a chemical compound with the molecular formula C14H12N4. It is a derivative of benzimidamide, featuring a 5-methylpyridin-2-yl group attached to the nitrogen atom. N-(5-methylpyridin-2-yl)benzimidamide is known for its potential applications in medicinal chemistry, particularly as a kinase inhibitor. It has been studied for its ability to target specific enzymes involved in cellular signaling pathways, which can be relevant for the development of therapeutics in various diseases. The compound's structure allows it to interact with the active sites of these enzymes, thereby modulating their activity. Its synthesis and biological evaluation are of interest to researchers in the field of drug discovery and development.

4999-40-0

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4999-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4999-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4999-40:
(6*4)+(5*9)+(4*9)+(3*9)+(2*4)+(1*0)=140
140 % 10 = 0
So 4999-40-0 is a valid CAS Registry Number.

4999-40-0Relevant academic research and scientific papers

The dearomative annulation between N -2-pyridylamidine and CO2 toward pyrido[1,2-a]-1,3,5-triazin-4-ones

Xia, Minfang,Hu, Weiming,Sun, Song,Yu, Jin-Tao,Cheng, Jiang

supporting information, p. 4064 - 4067 (2017/07/10)

A base-promoted dearomative annulation between N-2-pyridylamidine and an atmospheric pressure of CO2 was developed, affording a series of pyrido[1,2-a]-1,3,5-triazin-4-ones in moderate to excellent yields. CO2 served as a carbonyl so

I2/KI-Mediated Oxidative N-N Bond Formation for the Synthesis of 1,5-Fused 1,2,4-Triazoles from N -Aryl Amidines

Song, Lina,Tian, Xianhai,Lv, Zhigang,Li, Ertong,Wu, Jie,Liu, Yangxue,Yu, Wenquan,Chang, Junbiao

, p. 7219 - 7225 (2015/07/28)

An I2/KI-mediated oxidative N-N bond formation reaction is described. This new and environmentally benign approach allows for the convenient synthesis of a variety of 1,2,4-triazolo[1,5-a]pyridines and other 1,5-fused 1,2,4-triazoles from readi

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