62935-72-2 Usage
Uses
Different sources of media describe the Uses of 62935-72-2 differently. You can refer to the following data:
1. A precursor to coumarin-type fluorescent reagents
2. Key intermidiate for the synthesis of fluorescence probes in chromatographic detection. Shows local anesthetic activity.
3. 7-Methoxycoumarin-4-acetic acid is a precursor to coumarin-type fluorescent reagents. It has been uses as fluorescent probe in preparation of two novel LysB29 selectively labeled fluorescent derivatives of human insulin, in the preparation of cell-penetrating peptide transportan 10 (tp10) and as fluorescent label for peptides.
Check Digit Verification of cas no
The CAS Registry Mumber 62935-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62935-72:
(7*6)+(6*2)+(5*9)+(4*3)+(3*5)+(2*7)+(1*2)=142
142 % 10 = 2
So 62935-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O5/c1-16-8-2-3-9-7(4-11(13)14)5-12(15)17-10(9)6-8/h2-3,5-6H,4H2,1H3,(H,13,14)
62935-72-2Relevant articles and documents
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Laskowski,Clinton
, p. 3987,3989 (1950)
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Synthesis of 2-(2-oxo-2H-chromen-4-yl)acetamides as potent acetylcholinesterase inhibitors and molecular insights into binding interactions
Kara, Jiraporn,Suwanhom, Paptawan,Wattanapiromsakul, Chatchai,Nualnoi, Teerapat,Puripattanavong, Jindaporn,Khongkow, Pasarat,Lee, Vannajan Sanghiran,Gaurav, Anand,Lomlim, Luelak
, (2019/07/08)
Sixteen novel coumarin-based compounds are reported as potent acetylcholinesterase (AChE) inhibitors. The most active compound in this series, 5a (IC50 0.04 ± 0.01 μM), noncompetitively inhibited AChE with a higher potency than tacrine and gala
Synthetic and Structural Studies on Novel 4,3′-Bicoumarins
Pujar, Kiran K.,Kulkarni, Manohar V.,Alawandi, Ganesh N.,Anilkumar,Basanagouda, Mahantesha
, p. 2043 - 2052 (2015/08/18)
A series of directly linked 4-3′ bicoumarins have been synthesized by both Knoevenagel and Perkin reactions. This single-step transformation was accomplished by the reaction of coumarin-4-acetates with substituted salicylaldehydes in presence of piperidin