75329-65-6 Usage
Chemical structure
A 1,3-diketone moiety with a benzyl ether substituent at the 1-position.
Usage
Commonly used as a reagent in organic synthesis.
Key intermediate
Serves as a key intermediate for the preparation of various pharmaceuticals and biologically active compounds.
Application in chalcone derivatives
Used in the preparation of chalcone derivatives.
Formation of heterocycles
Utilized in the formation of heterocycles.
Antifungal properties
Studied for its potential antifungal properties.
Antibacterial properties
Investigated for its potential antibacterial properties.
Versatility
A versatile chemical with various applications in the field of organic chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 75329-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75329-65:
(7*7)+(6*5)+(5*3)+(4*2)+(3*9)+(2*6)+(1*5)=146
146 % 10 = 6
So 75329-65-6 is a valid CAS Registry Number.
75329-65-6Relevant articles and documents
Ru-Catalyzed Chemo- and Enantioselective Hydrogenation of β-Diketones Assisted by the Neighboring Heteroatoms
Li, Wanfang,Lu, Bin,Xie, Xiaomin,Zhang, Zhaoguo
supporting information, p. 5509 - 5513 (2019/08/01)
A highly chemo- and enantioselective hydrogenation of β-diketones was achieved by using [Ru(benzene)(S)-SunPhosCl]Cl for consistency in THF. The neighboring heteroatoms played important roles in guaranteeing the reactivity and controlling the chemoselectivity. These results suggested a potential approach for the clean and facile synthesis of functionalized chiral β-hydroxy ketones, which could otherwise be prepared through much less step-economic transformations.
