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3-(4-methoxyphenoxy)-4-oxo-2-(trifluoromethyl)-4H-chromen-7-yl cyclopropanecarboxylate is a complex organic compound with the molecular formula C20H15F3O5. It is a derivative of the chromen-4-one class of compounds, characterized by the presence of a cyclopropanecarboxylate group attached to the 7-yl position of the chromen-4-one core. The structure features a 4-methoxyphenoxy group at the 3-position and a trifluoromethyl group at the 2-position, which contribute to its unique chemical properties. 3-(4-methoxyphenoxy)-4-oxo-2-(trifluoromethyl)-4H-chromen-7-yl cyclopropanecarboxylate is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. Its specific chemical reactivity, stability, and biological activity are areas of interest for researchers, as these properties can influence its suitability for specific therapeutic uses.

5279-30-1

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5279-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5279-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5279-30:
(6*5)+(5*2)+(4*7)+(3*9)+(2*3)+(1*0)=101
101 % 10 = 1
So 5279-30-1 is a valid CAS Registry Number.

5279-30-1SDS

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 [3-(4-methoxyphenoxy)-4-oxo-2-(trifluoromethyl)chromen-7-yl] cyclopropanecarboxylate

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenoxy)-4-oxo-2-(trifluoromethyl)-4H-chromen-7-yl cyclopropanecarboxylate

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

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More Details:5279-30-1 SDS

5279-30-1Upstream product

5279-30-1Downstream Products

5279-30-1Relevant academic research and scientific papers

Sulfur Tuning of [1,3]-Dioxolo[4.5-f]benzodioxole (DBD) Fluorescent Dyes

Wessig, Pablo,John, Leonard,Sperlich, Eric,Kelling, Alexandra

, p. 499 - 511 (2021)

The replacement of oxygen by sulfur atoms of [1,3]-dioxolo[4.5-f]benzodioxole (DBD) fluorescent dyes is an efficient way to adjust the photophysical properties (sulfur tuning). While previously developed S4-DBD dyes exhibit considerably red-shifted absorption and emission wavelength, the heavy atom effect of four sulfur atoms cause low fluorescence quantum yields and short fluorescence lifetimes. Herein, we demonstrate that the replacement of less than four sulfur atoms (S1-DBD, 1,2-S2-DBD, and 1,4-S2-DBD dyes) permits a fine-tuning of the photophysical properties. In some cases, a similar influence on the wavelength without the detrimental effect on the quantum yields and lifetimes is observed. Furthermore, the synthetic accessibility of S1- and S2-DBD dyes is improved, compared with S4-DBD dyes. For coupling with biomolecules a series of reactive derivatives of the new dyes were developed (azides, OSu esters, alkynes, maleimides).

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