40322-49-4 Usage
Description
(4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is a chemical compound belonging to the class of benzothiepin derivatives. It is characterized by its potential therapeutic applications, particularly in the treatment of conditions such as depression and anxiety. (4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is notable for its ability to modulate the activity of specific neurotransmitters in the brain, which can lead to improvements in mood and emotional well-being. Furthermore, it is also being explored for its anti-inflammatory and neuroprotective properties, making it a promising candidate in drug development and medical research.
Uses
Used in Pharmaceutical Research:
(4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is used as a therapeutic agent for the treatment of conditions such as depression and anxiety. Its application is based on its ability to modulate neurotransmitter activity in the brain, which can positively impact mood and emotional well-being.
Used in Neurotransmitter Modulation:
In the field of neuroscience, (4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is used as a modulator of neurotransmitter activity. This application is due to its capacity to interact with and influence the levels and functions of certain neurotransmitters, which play a crucial role in regulating mood and emotional responses.
Used in Anti-inflammatory Applications:
(4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is also being investigated for its potential use as an anti-inflammatory agent. Its application in this area is driven by its ability to reduce inflammation, which can be beneficial in managing various conditions associated with inflammation.
Used in Neuroprotection:
In the context of neurodegenerative diseases, (4E)-4-ethylidene-3,4-dihydro-1-benzothiepin-5(2H)-one is being explored for its neuroprotective properties. Its application is based on the compound's potential to protect neurons from damage and degeneration, which could be valuable in the development of treatments for conditions such as Alzheimer's disease and Parkinson's disease.
Check Digit Verification of cas no
The CAS Registry Mumber 40322-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,2 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40322-49:
(7*4)+(6*0)+(5*3)+(4*2)+(3*2)+(2*4)+(1*9)=74
74 % 10 = 4
So 40322-49-4 is a valid CAS Registry Number.
40322-49-4Relevant articles and documents
Chelation-assisted intramolecular hydroacylation: Synthesis of medium ring sulfur heterocycles
Bendorf, Holly D.,Colella, Christine M.,Dixon, Elizabeth C.,Marchetti, Melissa,Matukonis, Alicia N.,Musselman, Jeffrey D.,Tiley, Tara A.
, p. 7031 - 7034 (2007/10/03)
Medium ring sulfur heterocycles are prepared from ω-alkenals and alkynals containing a sulfur tether atom via a novel chelation-assisted intramolecular hydroacylation catalyzed by rhodium(I).
