7570-37-8 Usage
Uses
Used in Biotechnology:
4-AMINO-4'-METHOXYSTILBENE is used as a fluorescent dye for the visualization of cellular components and biomolecules due to its blue fluorescence emission upon ultraviolet light excitation.
Used in Immunoassays:
In the field of immunoassays, 4-AMINO-4'-METHOXYSTILBENE serves as a fluorescent label, enabling the detection and quantification of specific biomolecules through its fluorescence properties.
Used in Cellular Imaging:
4-AMINO-4'-METHOXYSTILBENE is utilized as a fluorescent probe in cellular imaging, allowing researchers to observe and study the structure and function of cells with enhanced clarity.
Used in Photodynamic Therapy:
4-AMINO-4'-METHOXYSTILBENE has been studied for its potential applications in photodynamic therapy, where its light-induced cytotoxic properties can be harnessed to target and destroy cancer cells upon exposure to specific wavelengths of light.
Check Digit Verification of cas no
The CAS Registry Mumber 7570-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7570-37:
(6*7)+(5*5)+(4*7)+(3*0)+(2*3)+(1*7)=108
108 % 10 = 8
So 7570-37-8 is a valid CAS Registry Number.
7570-37-8Relevant academic research and scientific papers
Evidence for two-photon absorption-induced ESIPT of chromophores containing hydroxyl and imino groups
Gao, Fang,Ye, Xiaojuan,Li, Hongru,Zhong, Xiaolin,Wang, Qi
experimental part, p. 1313 - 1324 (2012/07/14)
This paper presents experimental and theoretical investigations into excited-state intramolecular proton transfer (ESIPT) in new chromophores with hydroxyl and imino groups under one- and two-photon excitation. The results show that internal hydrogen bond
N-ACYLAMINOBENZENE DERVATIVES AS SELECTIVE MONOAMINE OXIDASE B INHIBITORS
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Page 36, (2008/06/13)
This invention relates to N-acylamino aryl derivatives of the general formula (I), wherein R1 is halogen, halogen-(C1-C6)-alkyl, cyano, C1-C6-alkoxy or halogen-(C1-C6)-alkoxy; R
