5351-37-1 Usage
Description
(1Z,2E)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one oxime is a chemical compound with the molecular formula C15H15NO2. It is an oxime derivative of chalcone, a natural product found in some plants known for its antioxidant and anti-inflammatory properties. (1Z,2E)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one oxime features a phenyl group and a methoxy group attached to a propenone backbone, along with an oxime group connected to the alpha carbon. Its potential applications in pharmaceuticals and drug development are promising due to its reported biological activities, such as anti-cancer and anti-microbial properties. However, further research is necessary to fully explore its potential uses and properties.
Uses
Used in Pharmaceutical Industry:
(1Z,2E)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one oxime is used as a pharmaceutical compound for its potential anti-cancer properties. It has shown biological activities that warrant investigation into its use as a therapeutic agent against cancer cells.
Used in Drug Development:
In drug development, (1Z,2E)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one oxime is utilized as a lead compound for the discovery of new drugs. Its anti-microbial properties also suggest potential applications in the development of antimicrobial agents to combat resistant strains of bacteria.
Check Digit Verification of cas no
The CAS Registry Mumber 5351-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5351-37:
(6*5)+(5*3)+(4*5)+(3*1)+(2*3)+(1*7)=81
81 % 10 = 1
So 5351-37-1 is a valid CAS Registry Number.
5351-37-1Relevant articles and documents
Copper-catalyzed rearrangement of N-aryl nitrones into epoxyketimines
Mo, Dong-Liang,Anderson, Laura L.
, p. 6722 - 6725 (2013/07/26)
Please pass the oxygen: A new method for the preparation of trans-α,β-epoxyketimines has been achieved through a copper-catalyzed rearrangement of (E)-α,β-unsaturated nitrones. The scope and tolerance of the method is evaluated and the synthetic utility of the products is demonstrated. The new transformation provides facile access to an unusual, densely functionalized intermediate that can be exploited for further synthetic application. Copyright
