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575-04-2

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575-04-2 Usage

Uses

Different sources of media describe the Uses of 575-04-2 differently. You can refer to the following data:
1. Fluorescent substrate for oxidoreductases, especially for Cytochrome P450.
2. 7-Methoxy-4-(trifluoromethyl)coumarin is a biochemical for proteomics research.

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

575-04-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methoxy-4-(trifluoromethyl)coumarin

1.2 Other means of identification

Product number -
Other names 7-methoxy-4-(trifluoromethyl)chromen-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:575-04-2 SDS

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.

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