575-04-2 Usage
Description
7-Methoxy-4-(trifluoromethyl)coumarin is a synthetic compound characterized by its unique molecular structure, which features a coumarin core with a methoxy group at the 7th position and a trifluoromethyl group at the 4th position. 7-Methoxy-4-(trifluoromethyl)coumarin is known for its distinct fluorescent properties and is widely utilized in various research and industrial applications due to its chemical stability and reactivity.
Uses
Used in Biochemical Research:
7-Methoxy-4-(trifluoromethyl)coumarin is used as a fluorescent substrate for oxidoreductases, particularly for Cytochrome P450. Its fluorescence allows researchers to monitor enzyme activity and study the mechanisms of redox reactions in biological systems.
Used in Proteomics Research:
In the field of proteomics, 7-Methoxy-4-(trifluoromethyl)coumarin serves as a valuable biochemical tool. It is employed for the detection and analysis of proteins, enabling researchers to identify and quantify specific proteins within complex biological samples. 7-Methoxy-4-(trifluoromethyl)coumarin's reactivity and fluorescence properties make it an essential component in the development of novel proteomic techniques and assays.
Check Digit Verification of cas no
The CAS Registry Mumber 575-04-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 575-04:
(5*5)+(4*7)+(3*5)+(2*0)+(1*4)=72
72 % 10 = 2
So 575-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H7F3O3/c1-16-6-2-3-7-8(11(12,13)14)5-10(15)17-9(7)4-6/h2-5H,1H3
575-04-2Relevant articles and documents
Novel trifluoromethylcoumarinyl urea derivatives: Synthesis, characterization, fluorescence, and bioactivity
Qiao, Lili,Hao, Shuanghong
, (2018/03/21)
A series of novel trifluoromethylcoumarinyl urea derivatives were designed, synthesized, and characterized by 1H-NMR, 13C-NMR, and HR-ESI-MS. The fluorescence spectra of the target compounds were recorded. The spectra show that most of the title compounds glow green with λmaxem of 500-517 nm, while compounds 5r, 5s, 5u, and 5l (compounds named by authors) glow violet with λmaxem of 381-443 nm. Moreover, the herbicidal and antifungal activities of the synthesized compounds were evaluated for their potential use as pesticides. The results indicate that compound 5f against the caulis of Amaranthus retroflexus and compounds 5j and 5l against the taproot of Digitaria sanguinalis are equivalent to the commercial herbicide Acetochlor. Nine of the title compounds are more antifungal than commercial fungicide Carbendazim against Botrytis cinerea.
