7433-02-5 Usage
Uses
Used in Pharmaceutical Development:
2,3-dihydro-4H-benzo[h]thiochromen-4-one is used as a lead compound in pharmaceutical development for its potential to be formulated into new drugs and therapeutic agents. Its antioxidant, anti-inflammatory, and antiproliferative properties make it a valuable candidate for treating various diseases and conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,3-dihydro-4H-benzo[h]thiochromen-4-one is utilized as a subject of research to explore its pharmacological properties and potential applications. Its unique structure allows for the investigation of its interactions with biological targets and the development of novel therapeutic strategies.
Used in Antioxidant Applications:
2,3-dihydro-4H-benzo[h]thiochromen-4-one is used as an antioxidant agent to combat oxidative stress and related conditions. Its ability to neutralize free radicals and protect cells from damage makes it a promising candidate for use in treatments aimed at preventing or mitigating oxidative stress-induced diseases.
Used in Anti-inflammatory Applications:
As an anti-inflammatory agent, 2,3-dihydro-4H-benzo[h]thiochromen-4-one is employed to reduce inflammation and associated symptoms. Its potential to modulate inflammatory pathways and alleviate inflammatory responses positions it as a candidate for the development of anti-inflammatory drugs.
Used in Antiproliferative Applications:
2,3-dihydro-4H-benzo[h]thiochromen-4-one is used as an antiproliferative agent in the context of cancer treatment. Its capacity to inhibit the proliferation of cancer cells and potentially slow tumor growth makes it a valuable component in the development of anticancer therapies.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic efficacy of 2,3-dihydro-4H-benzo[h]thiochromen-4-one, it is utilized in conjunction with various drug delivery systems. These systems, which may include organic and metallic nanoparticles, aim to improve the compound's delivery to target sites, ensuring optimal pharmacological effects and minimizing side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 7433-02-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7433-02:
(6*7)+(5*4)+(4*3)+(3*3)+(2*0)+(1*2)=85
85 % 10 = 5
So 7433-02-5 is a valid CAS Registry Number.
7433-02-5Relevant academic research and scientific papers
CONFORMATIONAL ANALYSIS AND PHOTOCHeMICAL BEHAVIOUR OF SULFOXIDES IN THE NAPHTHOTHIOPYRAN AND NAPHTHOTHIOPYRAN SERIES
Still, Ian W. J.,Arora, Parkash C.,Hasan, S. Khaquan,Kutney, Gerald W.,Lo, LAwrence Y. T.,Turnbull, Kenneth
, p. 199 - 209 (2007/10/02)
The sulfoxides derived from 2,3-dihydro-4H-naphthothiopyran and its 4-phenyl and 4-oxo derivatives, as well as the analogous sulfoxides in the 2,3-dihydro-1H-naphthothiopyran series, have been synthesized and their structures established by spectroscopic methods, especially 1H and 13C nmr.On the photolysis these sulfoxides have been found to react by a rather inefficient photochemical deoxygenation pathway.
