439614-58-1 Usage
Description
1-(2-CHLORO-PHENYL)-ISOQUINOLINE is a chemical compound belonging to the isoquinoline class, characterized by its molecular formula C17H11ClN. It features a chlorophenyl group attached to the isoquinoline ring structure, which may contribute to its potential applications in pharmaceutical research and drug development. 1-(2-CHLORO-PHENYL)-ISOQUINOLINE has structural features that could be harnessed for various biological activities, such as anti-cancer, anti-microbial, and anti-inflammatory properties.
Uses
Used in Pharmaceutical Research and Drug Development:
1-(2-CHLORO-PHENYL)-ISOQUINOLINE is used as a compound of interest for pharmaceutical research and drug development due to its unique structural features and potential biological activities. Its chlorophenyl group and isoquinoline ring structure may offer opportunities for the development of new therapeutic agents.
Used in Anticancer Applications:
Within the pharmaceutical industry, 1-(2-CHLORO-PHENYL)-ISOQUINOLINE is used as a potential anticancer agent. Its isoquinoline derivatives have been studied for their anti-cancer properties, which could be further explored and developed for the treatment of various types of cancer.
Used in Anti-microbial Applications:
1-(2-CHLORO-PHENYL)-ISOQUINOLINE is also used as a potential anti-microbial agent. Its isoquinoline derivatives have shown anti-microbial properties, making it a candidate for the development of new antibiotics or antifungal agents to combat drug-resistant infections.
Used in Anti-inflammatory Applications:
In the field of inflammation and pain management, 1-(2-CHLORO-PHENYL)-ISOQUINOLINE is used as a potential anti-inflammatory agent. Its isoquinoline derivatives have demonstrated anti-inflammatory properties, which could be leveraged to develop new treatments for conditions characterized by inflammation, such as arthritis or other autoimmune disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 439614-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 439614-58:
(8*4)+(7*3)+(6*9)+(5*6)+(4*1)+(3*4)+(2*5)+(1*8)=171
171 % 10 = 1
So 439614-58-1 is a valid CAS Registry Number.
439614-58-1Relevant articles and documents
Cu-catalyzed direct ortho-chlorination/-oxygenation of aryls: Switching of oxidant, control the diversity of products
Botla, Vinayak,Akudari, Ashok,Malapaka, Chandrasekharam
supporting information, p. 115 - 119 (2018/12/05)
Highly regioselective copper catalyzed ortho-chlorination of aryl pyridines was achieved with TBHP as oxidant and 1,2-dichloroethane as chlorinating agent for the first time. Switching the oxidant from TBHP to benzoyl peroxide under identical reaction conditions effects ortho-oxygenation.
Copper-catalyzed aromatic C-H bond halogenation using lithium halides as halogenating reagents
Lu, Yongzhong,Wang, Ruiping,Qiao, Xixue,Shen, Zengming
supporting information; experimental part, p. 1038 - 1042 (2011/06/19)
The copper-catalyzed C-H halogenation of 2-aryl-pyridines containing a variety of electron-withdrawing and electron-donating substituents was described. It is worth noting that cheap and easy-to-handle lithium halides were utilized as the halogen sources. Georg Thieme Verlag Stuttgart · New York.
A simple catalytic method for the regioselective halogenation of arenes
Kalyani, Dipannita,Dick, Allison R.,Anani, Waseem Q.,Sanford, Melanie S.
, p. 2523 - 2526 (2007/10/03)
This paper describes a mild palladium-catalyzed method for the regioselective chlorination, bromination, and iodination of arene C-H bonds using N-halosuccinimides as oxidants. These transformations have been applied to a wide array of substrates and can provide products that are complementary to those obtained via conventional electrophilic aromatic substitution reactions.
