23042-77-5 Usage
Description
1-(2-Amino-5-methoxy-phenyl)-ethanone, also known as 5-Methoxy-2-aminoacetophenone, is a chemical compound with the molecular formula C9H11NO2. It is a derivative of acetophenone and is characterized by its potential biological activities, including antimicrobial and anticancer properties. 1-(2-Amino-5-methoxy-phenyl)-ethanone serves as a building block in the preparation of various pharmaceutical products and is a promising candidate in the development of new drug candidates for the treatment of different diseases.
Uses
Used in Pharmaceutical Research:
1-(2-Amino-5-methoxy-phenyl)-ethanone is used as a building block in the pharmaceutical industry for the synthesis of various pharmaceutical products. Its unique chemical structure allows for the creation of a wide range of compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(2-Amino-5-methoxy-phenyl)-ethanone is utilized as a key intermediate in the synthesis of complex organic molecules. Its versatile structure makes it a valuable component in the development of new chemical entities.
Used in Antimicrobial Applications:
1-(2-Amino-5-methoxy-phenyl)-ethanone has demonstrated antimicrobial properties, making it a potential candidate for use in the development of new antimicrobial agents. This application is particularly relevant in the context of increasing antibiotic resistance and the need for novel treatments.
Used in Anticancer Applications:
1-(2-Amino-5-methoxy-phenyl)-ethanone has shown potential anticancer properties, indicating its use in the development of new drug candidates for the treatment of various types of cancer. Further research is needed to fully understand its mechanisms of action and optimize its therapeutic potential.
Used in Drug Development:
1-(2-Amino-5-methoxy-phenyl)-ethanone is employed in the development of new drug candidates for the treatment of a variety of diseases. Its unique chemical structure and potential biological activities make it a valuable starting point for the design and synthesis of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 23042-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23042-77:
(7*2)+(6*3)+(5*0)+(4*4)+(3*2)+(2*7)+(1*7)=75
75 % 10 = 5
So 23042-77-5 is a valid CAS Registry Number.
23042-77-5Relevant articles and documents
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Sami Khan,La Montagne
, p. 1005,1007 (1979)
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WDR5 INHIBITORS AND MODULATORS
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Paragraph 00253, (2021/05/15)
Isoquinolmone compounds and derivatives inhibit WDR5 and associated protein-protein interactions, and the compounds and their pharmaceutical compositions are useful for treating disorders and conditions in a subject, such as cancer cell proliferation.
Experimental and Computational Studies on Cp*CyRh(III)/KOPiv-Catalyzed Intramolecular Dehydrogenative Cross-Couplings for Building Eight-Membered Sultam/Lactam Frameworks
Li, Liping,Gao, Hui,Sun, Ming,Zhou, Zhi,Yi, Wei
, p. 5473 - 5478 (2020/07/14)
Described herein is an unusual Cp*CyRh(III)-catalyzed intramolecular site-specific aryl C-H annulation, a highly chemoselective protocol providing direct access to eight-membered sultams/lactams with broad substrate/functional group tolerance. Experimental and computational studies reveal that such a transformation involves a unique PivOH-assisted aryl C-H activation/alkene insertion/β-H elimination/hydrogen-transfer process involving the Rh(III)-hydride species as the active intermediate with the concomitant release of H2 as the major byproduct, thus enabling the developed Cp*CyRh(III) catalysis with redox-neutral and highly atom-economical features.
