64700-15-8 Usage
Description
7-(Carboxymethoxy)-4-methylcoumarin (CMC) is an organic compound that belongs to the class of coumarins. It is characterized by its unique chemical structure, which features a carboxylate ester group and a methyl group attached to the coumarin core. 7-(CARBOXYMETHOXY)-4-METHYLCOUMARIN is known for its potential applications in various fields due to its distinct properties.
Uses
Used in Photochemistry:
7-(Carboxymethoxy)-4-methylcoumarin is used as a photosensitive agent in the preparation of poly(4-vinyl pyridine)-CMC, a photosensitive polymer. This application takes advantage of CMC's ability to absorb light and generate reactive species, which can initiate polymerization reactions.
Used in Analytical Chemistry:
CMC is used as a component in the synthesis of 3-chloro-7-[(chlorocarbonyl)methoxy]-4-methylcoumarin, which serves as a valuable intermediate in the development of various analytical reagents and probes.
Used in Fluorescent Probes:
7-(Carboxymethoxy)-4-methylcoumarin is used in the development of a novel fluorescent probe, Tb(III)-(7-carboxymethoxy-4-methylcoumarin) complex, for sensing of DNA. This application leverages the compound's fluorescent properties to detect and analyze DNA sequences, which can be useful in molecular biology and diagnostics.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, CMC can be utilized as a building block or intermediate for the synthesis of various drug candidates. Its unique chemical structure may contribute to the development of new therapeutic agents with potential applications in treating different diseases.
Used in Material Science:
CMC's properties may also find applications in the field of material science, where it could be used to develop new materials with specific optical, electronic, or mechanical properties. This could include the creation of advanced sensors, optoelectronic devices, or other high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 64700-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,0 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64700-15:
(7*6)+(6*4)+(5*7)+(4*0)+(3*0)+(2*1)+(1*5)=108
108 % 10 = 8
So 64700-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O5/c1-7-4-12(15)17-10-5-8(2-3-9(7)10)16-6-11(13)14/h2-5H,6H2,1H3,(H,13,14)/p-1
64700-15-8Relevant articles and documents
Phenacyl ester derivatives bearing heterocycles as models for photocleavable linkers: Synthesis and photolysis studies
Fonseca, Andrea S.C.,Gon?alves, M. Sameiro T.,Costa, Susana P.G.
experimental part, p. 8024 - 8032 (2012/09/25)
The synthesis of several phenacyl ester derivatives linked to oxygen and nitrogen heterocycles, benzoquinolone and (benzo)coumarins, was carried out in an effort to obtain systems that could be applied as photocleavable (bi)functional linkers for solid phase peptide synthesis. The heterocycles were attached to a spacer, with different lengths, followed by coupling to 2-bromo-1-phenylpropan-1-one, acting as a model for the solid support. Photolysis studies of the resulting phenacyl ester derivatives were carried out by irradiation in a photochemical reactor at different wavelengths (300, 350 and 419 nm), in methanol/HEPES buffer solution (80:20).
