Welcome to LookChem.com Sign In|Join Free
  • or
(2E)-1-(5-chloro-2-hydroxyphenyl)-3-furan-2-ylprop-2-en-1-one, also known as curcumenol, is a natural compound belonging to the class of curcuminoids found in the rhizomes of Curcuma longa (turmeric). It is known for its antioxidant and anti-inflammatory properties and has been studied for its potential therapeutic effects.
Used in Pharmaceutical Industry:
Curcumenol is used as a therapeutic agent for its potential ability to inhibit the growth of cancer cells, reduce inflammation, and protect against oxidative stress. It is also being investigated for its potential use in the treatment of neurodegenerative diseases and as a possible antimicrobial agent.
Used in Skincare Industry:
Curcumenol is used as an ingredient in skincare products for its anti-aging and skin-lightening properties.

7209-79-2

Post Buying Request

7209-79-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7209-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7209-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7209-79:
(6*7)+(5*2)+(4*0)+(3*9)+(2*7)+(1*9)=102
102 % 10 = 2
So 7209-79-2 is a valid CAS Registry Number.

7209-79-2SDS

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 (E)-1-(5-chloro-2-hydroxyphenyl)-3-(furan-2-yl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 5'-Chlor-2'-hydroxy-furfuryliden-chalkon

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:7209-79-2 SDS

7209-79-2Relevant academic research and scientific papers

Linking Flavonoids to Gold - A New Family of Gold Compounds for Potential Therapeutic Applications

Mirzadeh, Nedaossadat,Privér, Steven H.,Abraham, Amanda,Shukla, Ravi,Bansal, Vipul,Bhargava, Suresh K.

, p. 4275 - 4279 (2015)

The flavone ligands 8-chloro-2-tetrahydrofuryl-1,4-benzopyrone and 8-chloro-2-(2-methyltetrahydrofuryl)-1,4-benzopyrone have been used to prepare the first examples of alkynyl phosphine gold compounds containing flavonoids which exhibit cytotoxicity towar

Evaluation of DPPH radical scavenging activity of 2-(furan-2′-yl)-3-hydroxy-4H-chromen-4-one and their derivatives

Kaur, Ranbir,Kaur, Kulvir,Bansal, Manisha

, p. 1921 - 1924 (2016/07/06)

The 2-(furan-2′-yl)-3-hydroxy-4H-chromen-4-one and their substituted derivatives with electron donating and electron withdrawing groups have been synthesized. Free radical scavenging activity has been studied using 2,2′-diphenyl-1-picrylhydrazine (DPPH).

Electromeric effect of substitution at 6 th position in 2-(Furan-2-yl)-3-hydroxy-4 H-chromen-4-one (FHC) on the absorption and emission spectra

Bansal, Manisha,Kaur, Ranbir

, p. 405 - 412 (2015/05/13)

Five 3-Hydroxychromones (3HCs), namely, 2-(furan-2-yl)-3-hydroxy-4H-chromen-4-one (FHC) and its four derivatives by substitution of -CH3, -OH, -NO2 and -Cl at 6th position were synthesized from their corresponding 2′-hydro

Development of novel pesticides based on phytoalexins: Part 2. Quantitative structure-activity relationships of 2-heteroaryl-4-chromanone derivatives

Yang, Guangfu,Jiang, Xiaohua,Yang, Huazheng

, p. 1063 - 1067 (2007/10/03)

Phytoalexins are low-molecular-weight chemicals that immune systems of plants produce and accumulate in response to infections, especially those of fungal origin. Although their content is not high in plants, yet they have shown unique fungicidal activity

On the Mechanism for the Phototransformation of 3-Alkoxy-2-(2'-furyl)-4-oxo-4H-1-benzopyrans

Gupta, Satish C.,Saini, Ashok,Kumar, Devinder,Yadav, Narender S.,Chand, Kuldeep,et al.

, p. 177 - 184 (2007/10/02)

Photoirradiation of 3-alkoxy-6-chloro-2-(2'-furyl)-4-oxo-4H-1-benzopyrans 3 led to the formation of methyl 8-chloro-10-oxo-2-phenyl-2,3,4,10-tetrahydropyranobenzopyran-3-ylacetate 4.The reaction proceeds through the formation of 8-chloro-4-pheny

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7209-79-2