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2-((4-(dimethylamino)phenylamino)methyl)phenol, also known as 4-(dimethylamino)phenylaminophenol, is an organic compound with the molecular formula C14H16N2O. It is a derivative of phenol, featuring a dimethylamino group attached to a phenyl ring, which is further connected to another phenyl ring through an amino group. 2-((4-(dimethylamino)phenylamino)methyl)phenol is characterized by its yellowish color and is used in various applications, including as an intermediate in the synthesis of dyes and pigments. Its chemical structure endows it with specific properties, such as its ability to form complexes, which makes it valuable in the chemical industry.

5713-64-4

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5713-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5713-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5713-64:
(6*5)+(5*7)+(4*1)+(3*3)+(2*6)+(1*4)=94
94 % 10 = 4
So 5713-64-4 is a valid CAS Registry Number.

5713-64-4Relevant academic research and scientific papers

Understanding difficulties of irregular number-membered ring transition states for intramolecular proton transfer in excited state

Qin, Xiaozhuan,Ding, Ge,Wang, Zhenqiang,Gong, Yulong,Gao, Fang,Zhang, Shengtao,Luo, Ziping,Li, Hongru

supporting information, p. 403 - 410 (2017/01/03)

This study presents a variety of organic dyes with similar molecular structures that could undergo intramolecular proton transfer in excited states via five-, six- and seven-number-membered ring transition states, respectively. In addition, the dyes without proton transfer segments are also synthesized to use as references. X-ray single crystal diffraction, NMR spectra as well as UV/visible spectra suggests the presence of internal hydrogen bond with different strength in the target dyes. The steady and transient fluorescence measurements demonstrate occurrence of excited state intramolecular proton transfer via a six number-membered ring transition state. In contrast, it cannot be processed through five- and seven-number-membered ring transition states of the studied dyes. The molecular geometry optimization of the studied dyes reveals fundamental factors for the difficulties of intramolecular proton transfer in excited states via five- and seven-number-membered ring transition states.

Synthesis and structure-antibacterial activity relationship studies of 4-substituted phenyl-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-thiones

Agirbas, Hikmet,Kemal, Berat,Budak, Fatma

experimental part, p. 1170 - 1180 (2012/05/05)

The synthesis and characterization of a series of 4-substituted phenyl-4,5-dihydrobenzo[f][1,4]oxazepin- 3(2H)-thiones were presented. Preliminary in vitro antimicrobial activity of the compounds was assessed against a panel of microorganisms including S.

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