51073-13-3 Usage
Description
(3,5-Dibromo-4-methoxyphenyl)(2-ethyl-3-benzofuranyl)-methanone is a synthetic organic compound characterized by a dibromo-substituted methoxyphenyl group and an ethyl-benzofuranyl group attached to a methanone functional group. This type of ketone contains bromine and methoxy groups, along with a benzofuran ring, and may have potential applications in organic chemistry, pharmaceuticals, or materials science, although its specific uses and properties are not well-known.
Used in Organic Chemistry:
(3,5-Dibromo-4-methoxyphenyl)(2-ethyl-3-benzofuranyl)-methanone is used as a synthetic intermediate for the development of new organic compounds due to its unique structure and functional groups.
Used in Pharmaceutical Industry:
(3,5-Dibromo-4-methoxyphenyl)(2-ethyl-3-benzofuranyl)-methanone is used as a potential pharmaceutical candidate for the development of new drugs, given its structural features that may offer novel therapeutic properties.
Used in Materials Science:
(3,5-Dibromo-4-methoxyphenyl)(2-ethyl-3-benzofuranyl)-methanone is used as a component in the research and development of new materials with specific properties, such as those with enhanced stability or reactivity.
Further research and testing would be needed to fully understand the potential uses and effects of this chemical compound in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51073-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51073-13:
(7*5)+(6*1)+(5*0)+(4*7)+(3*3)+(2*1)+(1*3)=83
83 % 10 = 3
So 51073-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H14Br2O3/c1-3-14-16(11-6-4-5-7-15(11)23-14)17(21)10-8-12(19)18(22-2)13(20)9-10/h4-9H,3H2,1-2H3
51073-13-3Relevant articles and documents
Cu-Catalyzed Site-Selective Benzylic Chlorination Enabling Net C–H Coupling with Oxidatively Sensitive Nucleophiles
Lopez, Marco A.,Buss, Joshua A.,Stahl, Shannon S.
supporting information, p. 597 - 601 (2022/01/20)
Site-selective chlorination of benzylic C–H bonds is achieved using a CuICl/bis(oxazoline) catalyst with N-fluorobenzenesulfonimide as the oxidant and KCl as a chloride source. This method exhibits higher benzylic selectivity, relative to estab
Compounds that modulate the activity of PTP-1B and TC-PTP
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Page/Page column 13, (2008/06/13)
The present invention relates to a new and improved method for treating diabetes and.or its associated complications by modulating the activity of protein tryosin phosphatase 1B (“PTP-1B”). The inventive compounds modulate the activity PTP-1B by binding t
