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4-[2-(4-chlorophenyl)ethenyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6280-47-3

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6280-47-3 Usage

General Description

4-[2-(4-chlorophenyl)ethenyl]phenol is a chemical compound with a molecular formula C16H12ClO. It is a derivative of resveratrol, a polyphenolic compound found in grapes and various plants. This chemical is often used in the production of cosmetics, personal care products, and dietary supplements due to its antioxidant and anti-inflammatory properties. It is also being studied for its potential applications in medical research and drug development. The presence of a chlorophenyl group in its structure gives it the ability to act as an inhibitor of certain enzymes and receptors, making it a valuable compound in various fields of research and product development.

Check Digit Verification of cas no

The CAS Registry Mumber 6280-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6280-47:
(6*6)+(5*2)+(4*8)+(3*0)+(2*4)+(1*7)=93
93 % 10 = 3
So 6280-47-3 is a valid CAS Registry Number.

6280-47-3SDS

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 4-[(E)-2-(4-chlorophenyl)ethenyl]phenol

1.2 Other means of identification

Product number -
Other names 4-Chlor-4'-hydroxy-stilben

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:6280-47-3 SDS

6280-47-3Downstream Products

6280-47-3Relevant academic research and scientific papers

Searching for new tools to counteract the helicobacter pylori resistance: The positive action of resveratrol derivatives

Di Fermo, Paola,Di Lodovico, Silvia,Amoroso, Rosa,De Filippis, Barbara,D’ercole, Simonetta,Di Campli, Emanuela,Cellini, Luigina,Di Giulio, Mara

, p. 1 - 16 (2020/12/17)

The drug-resistance phenomenon in Helicobacter pylori underlines the need of novel strategies to improve the eradication rate including alternative treatments combining antibiotic and non-antibiotic compounds with synergistic action. In this study, the antibacterial (MIC/MBC) and anti-virulence effects (biofilm reduction and swarming motility inhibition) of resveratrol-RSV and new synthetized RSV-phenol derivatives, with a higher bioavailability, alone and combined with levofloxacin-LVX were evaluated against resistant H. pylori clinical strains. The experiments were confirmed in vivo using the Galleria mellonella model. Among the studied RSV derivatives, RSV-3 and RSV-4 possessed higher antibacterial activity with respect to RSV (MICs from 6.25 to 200 μg/mL and from 3.12 to 200 μg/mL, respectively). RSV, RSV-3, and RSV-4 were able to synergize with LVX restoring its effect in two out of seven clinical resistant strains tested for the study. RSV, RSV-3, and RSV-4, alone and with LVX at sub-MIC and sub-synergistic concentrations, significantly reduced the biofilm formation. Moreover, RSV-3 and RSV-4 reduced the H. pylori swarming motility on soft agar. RSV, RSV-3, and RSV-4 were non-toxic for G. mellonella larvae and displayed a protective effect against H. pylori infection. Overall, RSV–phenol derivatives should be considered interesting candidates for innovative therapeutic schemes to tackle the H. pylori antibiotic resistance.

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