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2-[2-(3-methoxyphenyl)ethyl]cyclohexane-1,3-dione is a complex organic compound with the molecular formula C16H18O3. It is a derivative of cyclohexane, featuring a 1,3-dione functional group, which consists of two carbonyl groups (C=O) separated by a single carbon atom. The compound also contains a 3-methoxyphenyl group, which is a phenyl ring (C6H5) with a methoxy (-OCH3) substituent at the 3rd position. The presence of this functional group imparts unique chemical and physical properties to the molecule, making it potentially useful in various chemical and pharmaceutical applications. The structure of 2-[2-(3-methoxyphenyl)ethyl]cyclohexane-1,3-dione is characterized by a cyclohexane ring with a 1,3-dione group and a 3-methoxyphenylethyl side chain, which contributes to its stability and reactivity.

6321-53-5

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6321-53-5 Usage

Molecular Weight

284.33

Chemical Class

Cyclohexanediones

Derivative of

Curcumin (found in turmeric)

Pharmaceutical Applications

Potential treatment for cancer, inflammation, and oxidative stress

Chemical Properties

+ Potent antioxidant and anti-inflammatory properties
+ Exhibits anticancer effects through various mechanisms

Importance in Medicinal Chemistry and Drug Discovery

Promising candidate for drug development and further research due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6321-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6321-53:
(6*6)+(5*3)+(4*2)+(3*1)+(2*5)+(1*3)=75
75 % 10 = 5
So 6321-53-5 is a valid CAS Registry Number.

6321-53-5SDS

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 2-[2-(3-methoxyphenyl)ethyl]cyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(3-methoxy-phenethyl)-cyclohexane-1,3-dione

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:6321-53-5 SDS

6321-53-5Relevant academic research and scientific papers

Cationic cyclization of 2-alkenyl-1,3-dithiolanes: Diastereoselective synthesis of trans-decalins

Goncalves, Sylvie,Santoro, Stefano,Nicolas, Marc,Wagner, Alain,Maillos, Philippe,Himo, Fahmi,Baati, Rachid

experimental part, p. 3274 - 3285 (2011/06/25)

An unprecedented and highly diastereoselective 6-endo-trig cyclization of 2-alkenyl-1,3-dithiolanes has been developed yielding trans-decalins, an important scaffold present in numerous di- and triterpenes. The novelty of this 6-endo-trig cyclization stan

Hypervalent iodine(III)-induced intramolecular cyclization of α-(aryl)alkyl-β-dicarbonyl compounds: A convenient synthesis of benzannulated and spirobenzannulated compounds

Arisawa,Ramesh,Nakajima,Tohma,Kita

, p. 59 - 65 (2007/10/03)

A novel hypervalent iodine(III)-induced direct intramolecular cyclization of α-(aryl)alkyl-β-dicarbonyl compounds has been described. Both meta- and para-substituted phenol ether derivatives containing acyclic or cyclic 1,3-dicarbonyl moieties at the side chain undergo this reaction in a facile manner. The reactions afford benzannulated and spirobenzannulated compounds that are of biological importance. The reaction is found to be general, mild, and high yielding. The mechanism of the reaction has been shown to involve a cation radical intermediate.

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