1214-20-6 Usage
General Description
2-Methoxyxanthen-9-one is a chemical compound with the molecular formula C14H10O3. It is a derivative of xanthene, and is commonly used as a yellow fluorescent dye. It is known for its light absorption and emission properties, making it useful for various applications such as in the field of organic electronics and optoelectronic devices. 2-Methoxyxanthen-9-one is also used in the development of fluorescent probes and indicators for biological imaging and diagnostics. Additionally, it has potential applications in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 1214-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1214-20:
(6*1)+(5*2)+(4*1)+(3*4)+(2*2)+(1*0)=36
36 % 10 = 6
So 1214-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O3/c1-16-9-6-7-13-11(8-9)14(15)10-4-2-3-5-12(10)17-13/h2-8H,1H3
1214-20-6Relevant articles and documents
Design, synthesis, and anticonvulsant activity of some derivatives of xanthone with aminoalkanol moieties
Waszkielewicz, Anna M.,S?oczyńska, Karolina,P?kala, El?bieta,?mudzki, Pawe?,Siwek, Agata,Grybo?, Anna,Marona, Henryk
, p. 339 - 352 (2017/04/03)
A series of new xanthone derivatives have been synthesized and evaluated for their anticonvulsant properties in the maximal electroshock, subcutaneous metrazole tests and for neurotoxicity in the rotarod in mice, i.p. and rats, p.o. Compound 9: R,S-2-{2-[(1-hydroxybutan-2-yl]amino)ethoxy}-9H-xanthen-9-one and compound 12: R,S-2-{3-[(1-hydroxybutan-2-yl)amino]propoxy}-9H-xanthen-9-one exerted activity in rats, p.o. 2 and 4?h after administration, respectively. Therefore, metabolic stability of the compounds was evaluated with use of rat microsomes, resulting in half-life t1/2 136 and 108?min, respectively, indicating that either the metabolites are very active or the parent compounds exert ADME properties other than metabolism which influence the late onset of activity.
