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6-chloro-2-(quinolin-2-yl)-4H-chromen-4-one is a complex organic compound with the molecular formula C17H10ClNO2. It is a derivative of the 4H-chromen-4-one class of molecules, which are characterized by a fused benzopyran ring system. This particular compound features a quinoline moiety (quinolin-2-yl) attached to the 2-position of the chromen-4-one core, and a chlorine atom at the 6-position. The presence of the chlorine atom and the quinoline ring impart unique chemical and potentially biological properties to the molecule. 6-chloro-2-(quinolin-2-yl)-4H-chromen-4-one may be of interest in medicinal chemistry due to the diverse range of activities associated with quinoline-containing compounds, such as antimalarial, anti-inflammatory, and anticancer effects. However, the specific applications and properties of 6-chloro-2-(quinolin-2-yl)-4H-chromen-4-one would require further investigation and characterization.

2508-13-6

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2508-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2508-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2508-13:
(6*2)+(5*5)+(4*0)+(3*8)+(2*1)+(1*3)=66
66 % 10 = 6
So 2508-13-6 is a valid CAS Registry Number.

2508-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-quinolin-2-ylchromen-4-one

1.2 Other means of identification

Product number -
Other names 6-chloro-2-quinolin-2-yl-chromen-4-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

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More Details:2508-13-6 SDS

2508-13-6Downstream Products

2508-13-6Relevant academic research and scientific papers

Temperature-Controlled Desulfonylative Condensation of α-Sulfonyl o-Hydroxyacetophenones and 2-Formyl Azaarenes: Synthesis of Azaaryl Aurones and Flavones

Chang, Meng-Yang,Chen, Han-Yu,Tsai, Yu-Lin

, p. 326 - 337 (2019/01/08)

Temperature-controlled intermolecular desulfonylative condensation of α-sulfonyl o-hydroxyacetophenones with 2-formyl azaarenes (pyridines and quinolones) provides azaaryl (pyridyl and quinolyl) aurones and flavones under warming and refluxing toluene reaction conditions via the formation of the intermediate of sulfonyl chroman-4-one. The uses of various solvents are investigated for facile and efficient transformation. A plausible mechanism is proposed.

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