40360-69-8 Usage
Description
(6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone is a synthetic organic molecule that features a 1,3-benzodioxole ring and a 2,3-dihydro-1H-indole ring connected to a methanone group. (6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone is recognized for its unique structural characteristics and potential biological activity, making it a promising candidate in the realms of medicinal and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
(6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone is utilized as a potential drug candidate in pharmaceutical research due to its structural features and possible pharmacological properties. (6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone's unique arrangement of the benzodioxole and dihydro-1H-indole rings, along with the presence of a bromine atom, make it an interesting target for chemical synthesis and biological evaluation.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone serves as a valuable compound for the development of new drugs. Its specific molecular structure allows for exploration into various therapeutic applications, potentially leading to the creation of novel medications with improved efficacy and reduced side effects.
Used in Neuroscience:
(6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone is also of interest in neuroscience, where it may be investigated for its potential to influence neurological processes or treat neurodegenerative diseases. (6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone's interaction with specific receptors or pathways in the nervous system could provide insights into the development of new therapeutic strategies for neurological disorders.
Used in Drug Discovery:
Within the context of drug discovery, (6-bromo-1,3-benzodioxol-5-yl)(2,3-dihydro-1H-indol-1-yl)methanone is employed as a starting point for the design and synthesis of new chemical entities. Its unique molecular framework offers opportunities for modification and optimization, potentially leading to the identification of more effective and selective drug candidates for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 40360-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,6 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40360-69:
(7*4)+(6*0)+(5*3)+(4*6)+(3*0)+(2*6)+(1*9)=88
88 % 10 = 8
So 40360-69-8 is a valid CAS Registry Number.
40360-69-8Relevant articles and documents
Intramolecular direct dehydrohalide coupling promoted by KOtBu: Total synthesis of amaryllidaceae alkaloids anhydrolycorinone and oxoassoanine
De, Subhadip,Ghosh, Santanu,Bhunia, Subhajit,Sheikh, Javeed Ahmad,Bisai, Alakesh
, p. 4466 - 4469 (2012/10/29)
A transition-metal-free intramolecular dehydrohalide coupling via intramolecular homolytic aromatic substitution (HAS) with aryl radicals has been developed in the presence of potassium tert-butoxide and an organic molecule as the catalyst. The methodology has been applied to a concise synthesis of Amaryllidaceae alkaloids viz. oxoassoanine (1b), anhydrolycorinone (1d), and other related structures. Interestingly, the method also works only in the presence of potassium tert-butoxide.
