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2',4',6'-Trimethoxychalcone is a naturally occurring chalcone compound characterized by the presence of three methoxy groups at the 2', 4', and 6' positions on the chalcone backbone. Chalcones are a class of flavonoids known for their diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties. This specific chalcone is found in various plants and has been studied for its potential health benefits and therapeutic applications. Research on 2',4',6'-trimethoxychalcone has shown promising results in terms of its ability to modulate cellular signaling pathways, inhibit certain enzymes, and protect against oxidative stress, making it a subject of interest in the field of natural product chemistry and pharmacology.

1159-58-6

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1159-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1159-58-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1159-58:
(6*1)+(5*1)+(4*5)+(3*9)+(2*5)+(1*8)=76
76 % 10 = 6
So 1159-58-6 is a valid CAS Registry Number.

1159-58-6Downstream Products

1159-58-6Relevant academic research and scientific papers

Design of potent fluoro-substituted chalcones as antimicrobial agents

Burmaoglu, Serdar,Algul, Oztekin,Gobek, Arzu,Aktas Anil, Derya,Ulger, Mahmut,Erturk, Busra Gul,Kaplan, Engin,Dogen, Aylin,Aslan, G?nül

, p. 490 - 495 (2017)

Owing to ever-increasing bacterial and fungal drug resistance, we attempted to develop novel antitubercular and antimicrobial agents. For this purpose, we developed some new fluorine-substituted chalcone analogs (3, 4, 9–15, and 20–23) using a structure–a

Enantioselective Ring Opening of meso-Epoxides with Silicon Tetrachloride Catalyzed by Pyridine N-Oxides Fused with the Bicyclo[3.3.1]nonane Framework

Neni?kis, Algirdas,Ston?ius, Sigitas

, p. 6359 - 6369 (2015/10/06)

The synthesis of new chiral Lewis basic organocatalysts that contain pyridine N-oxide moieties fused with the bicyclo[3.3.1]nonane framework is reported. The obtained pyridine N-oxides were employed as catalysts in the enantioselective ring opening of meso-epoxides with silicon tetrachloride. Derivative 1b endowed with two 2,4-diaryl-substituted pyridine N-oxide moieties proved to be a particularly effective catalyst for desymmetrization of norbornene oxide 16i to furnish Wagner-Meerwein rearrangement product 20i in unprecedented 96 % ee. Difunctional congener 3, which is striped of the 4-aryl substituents, exhibited moderate to high levels of asymmetric induction (47-88 % ee) with alicyclic epoxide substrates. Chiral Lewis basic catalysts with pyridine N-oxide moieties fused with a bicyclo[3.3.1]nonane framework were used in the enantioselective ring opening of meso-epoxides. 2,4-Diaryl-substituted N-oxide exhibited excellent asymmetric induction with norbornene oxide (96 % ee), whereas less-substituted congener was most effective with alicyclic epoxide substrates (47-88 % ee).

NUCLEAR RECEPTOR MODULATORS AND THEIR USE FOR THE TREATMENT AND PREVENTION OF CANCER

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Page/Page column 25, (2013/02/28)

Disclosed are compounds which are nuclear receptor modulators that can act as antagonists to the androgen receptor, for example, a compound of Formula I: wherein R1 to R5 and X1 to X5 are as described herein, as well as pharmaceutically acceptable salts, solvates, and stereoisomers thereof. Pharmaceutical compositions comprising such compounds, as well as methods of use, and treatment for cancers, including prostate cancers, other nuclear receptor mediated cancers, and other conditions, are also disclosed.

Zinc oxide as a regioselective and heterogeneous catalyst for the synthesis of chalcones at room temperature

More, Parmeshwar E.,Bandgar, Babasaheb P.,Kamble, Vinod T.

, p. 30 - 32 (2012/10/30)

Zinc oxide catalyzed synthesis of chalcones has been carried out under solvent-free conditions at room temperature. Activated as well as unactivated aromatics smoothly underwent Friedel-Crafts acylation with α, β-unsaturated acid chlorides furnishing excellent yields of the corresponding chalcones. The zinc oxide can be recovered and reused at least three times without any appreciable loss in activity.

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