61658-90-0 Usage
Uses
Used in Pharmaceutical Industry:
(3Z)-3-ethylidene-2-benzofuran-1(3H)-one is used as a key intermediate in the synthesis of various drugs, agrochemicals, and bioactive compounds. Its unique molecular structure and reactivity make it a valuable component in the development of new pharmaceutical products.
Used in Organic Synthesis:
(3Z)-3-ethylidene-2-benzofuran-1(3H)-one is used as a building block in the synthesis of complex organic molecules. Its distinct aromatic odor and unique reactivity make it a useful component in the creation of novel organic compounds.
Used in Antioxidant Applications:
(3Z)-3-ethylidene-2-benzofuran-1(3H)-one has been studied for its potential antioxidant properties. Its ability to neutralize free radicals and protect cells from oxidative damage makes it a promising candidate for use in antioxidant formulations.
Used in Anticancer Applications:
(3Z)-3-ethylidene-2-benzofuran-1(3H)-one has also been studied for its potential anticancer properties. Its unique molecular structure and reactivity may contribute to its ability to inhibit the growth and proliferation of cancer cells, making it a potential candidate for use in cancer treatment.
Overall, (3Z)-3-ethylidene-2-benzofuran-1(3H)-one has garnered significant interest in both the scientific and industrial communities due to its versatile applications and potential therapeutic benefits. Its unique properties and reactivity make it a valuable compound for use in various industries, including pharmaceuticals, organic synthesis, and potentially as a therapeutic agent.
Check Digit Verification of cas no
The CAS Registry Mumber 61658-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,5 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61658-90:
(7*6)+(6*1)+(5*6)+(4*5)+(3*8)+(2*9)+(1*0)=140
140 % 10 = 0
So 61658-90-0 is a valid CAS Registry Number.
61658-90-0Relevant academic research and scientific papers
Catalytic enantioselective synthesis of chiral phthalides by efficient reductive cyclization of 2-acylarylcarboxylates under aqueous transfer hydrogenation conditions
Zhang, Bo,Xu, Ming-Hua,Lin, Guo-Qiang
supporting information; experimental part, p. 4712 - 4715 (2009/12/08)
A new diamine ligand for asymmetric transfer hydrogenation (ATH) was discovered. The reductive cyclization of 2-acylarylcarboxylates was found to proceed highly stereoselective by the new Ru complex-catalyzed ATH and subsequent In situ lactonization under aqueous conditions. It enables efficient access to a wide variety of 3-substituted phthalides In enantiomerically pure form.
