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4-Flavanthione is a chemical compound belonging to the class of flavans, which are a type of flavonoid. It is characterized by a sulfur-containing heterocyclic ring, specifically a thione group, attached to the flavan core structure. 4-flavanthione is known for its potential antioxidant properties and is found in various plants, contributing to their defense mechanisms against oxidative stress. 4-Flavanthione's chemical structure is defined by a carbon-carbon double bond between the 2 and 3 positions, a hydroxyl group at the 3 position, and a sulfur atom double-bonded to the 4 position, which is part of the thione group. Its unique structure and properties make it a subject of interest in the study of natural products and their potential applications in medicine and nutrition.

4431-44-1

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4431-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4431-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4431-44:
(6*4)+(5*4)+(4*3)+(3*1)+(2*4)+(1*4)=71
71 % 10 = 1
So 4431-44-1 is a valid CAS Registry Number.

4431-44-1Relevant academic research and scientific papers

One-Pot Catalytic Cleavage of C=S Double Bonds by Pd Catalysts at Room Temperature

Zhu, Ting,Wu, Xiaoxi,Yang, Xinzheng,Sharma, Bigyan,Li, Na,Huang, Jiaming,Wang, Wentao,Xing, Wang,Zhao, Zhenwen,Huang, Hui

, p. 9266 - 9273 (2018)

The C=S double bonds in CS2 and thioketones were catalytically cleaved by Pd dimeric complexes [(N∧N)2Pd2(NO3)2](NO3)2 (N∧N, 2,2′-bipyridine, 4,4′-dimethylbipyridine or 4,4′-bis(trifluoromethyl)) at room temperature in one pot to afford CO2 and ketones, respectively, for the first time. The mechanisms were fully investigated by kinetic NMR, isotope-labeled experiments, in situ ESI-MS, and DFT calculations. The reaction is involved a hydrolytic desulfurization process to generate C=O double bonds and a trinuclear cluster, which plays a pivotal role in the catalytic cycle to regenerate the dimeric catalysts with HNO3. Furthermore, the electronic properties of catalyst ligands possess significant influence on reaction rates and kinetic parameters. At the same temperature, the reaction rate is consistent with the order of electronegativity of N∧N ligands (4,4′-bis(trifluoromethyl) > 2,2′-bipyridine > 4,4′-dimethylbipyridine). This homogeneous catalytic reaction features mild conditions, a broad substrate scope, and operational simplicity, affording insight into the mechanism of catalytic activation of carbon sulfur bonds.

Chemotherapeutic agents

-

, (2008/06/13)

A method of treating or preventing viral infections, in particular rhinovirus infections comprising the administration of an effective amount of a 2-phenyltetralin derivative or a heterocyclic analogue thereof. Pharmaceutical compositions containing these compounds, and some novel compounds are also disclosed.

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