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5-Methoxy-2-phenyl-4H-thiochromen-4-one is a chemical compound belonging to the class of thiochromen-4-ones, characterized by a fused thiochromene ring system. 5-methoxy-2-phenyl-4H-thiochromen-4-one features a 4H-thiochromen-4-one core, with a methoxy group at the 5-position and a phenyl group at the 2-position. It is an organic molecule with potential applications in pharmaceuticals and materials science, particularly in the development of new drugs and chemical compounds. The specific properties and reactivity of 5-methoxy-2-phenyl-4H-thiochromen-4-one are influenced by the presence of the thiochromene ring, the methoxy group, and the phenyl substituent, which can affect its electronic properties, solubility, and potential interactions with other molecules.

86406-07-7

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86406-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86406-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,0 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86406-07:
(7*8)+(6*6)+(5*4)+(4*0)+(3*6)+(2*0)+(1*7)=137
137 % 10 = 7
So 86406-07-7 is a valid CAS Registry Number.

86406-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-2-phenylthiochromen-4-one

1.2 Other means of identification

Product number -
Other names Y6435

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:86406-07-7 SDS

86406-07-7Relevant academic research and scientific papers

Antitumor agents. 166. Synthesis and biological evaluation of 5,6,7,8-substituted-2-phenylthiochromen-4-ones

Wang, Hui-Kang,Bastow, Kenneth F.,Cosentino, L. Mark,Lee, Kuo-Hsiung

, p. 1975 - 1980 (2007/10/03)

As a continuation of our structure-activity relationship study of substituted 2-phenyl-4-quinolones and flavonoids as antitumor and antiviral agents, a series of 5,6,7,8-substituted-2-phenylthiochromen-4-ones has been synthesized by condensation of substi

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