185407-41-4 Usage
Description
(7-METHOXY-1-BENZOFURAN-2-YL)(PHENYL)METHANONE, with a molecular formula C15H11O3, is a chemical compound that is a ketone derivative of phenyl and benzofuran. It features a benzofuran moiety, which can exhibit various biological activities, and a phenyl group, suggesting potential for interactions with biological targets. This makes it a promising candidate for further investigation in medicinal chemistry and drug design.
Uses
Used in Organic Synthesis:
(7-METHOXY-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is used as an intermediate in organic synthesis for the creation of various chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (7-METHOXY-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is used as a research compound for exploring its potential in drug discovery and development.
Used in Drug Design and Development:
(7-METHOXY-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is used as a valuable compound in drug design and development due to its potential interactions with biological targets and its promising biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 185407-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 185407-41:
(8*1)+(7*8)+(6*5)+(5*4)+(4*0)+(3*7)+(2*4)+(1*1)=144
144 % 10 = 4
So 185407-41-4 is a valid CAS Registry Number.
185407-41-4Relevant articles and documents
Synthesis method of benzofuran compound
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Paragraph 0053-0060; 0062; 0063, (2021/05/19)
The invention belongs to the field of organic chemical synthesis, and particularly relates to a synthesis method of a benzofuran compound. According to the invention, the reaction system adopts economical and efficient iron phthalocyanine as a catalyst, a
An expedient synthesis of enantioenriched substituted (2-benzofuryl) arylcarbinols via tandem Rap-Stoermer and asymmetric transfer hydrogenation reactions
Kumaraswamy, Gullapalli,Ramakrishna, Gajula,Raju, Ragam,Padmaja, Mogilisetti
experimental part, p. 9814 - 9818 (2011/02/22)
An expedient synthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap-Stoermer reaction/catalytic asymmetric tra