521-73-3 Usage
Uses
Used in Pharmaceutical Industry:
ISOQUINOLINE-1,3,4-TRIONE is used as a chelating agent and antioxidant for its anti-tumor, anti-inflammatory, and anti-oxidative properties. It is employed in the development of therapeutic agents targeting various health conditions.
Used in Cosmetic Industry:
In the cosmetic industry, ISOQUINOLINE-1,3,4-TRIONE is used as an active ingredient for its skin-friendly properties, including its anti-inflammatory and anti-oxidative effects, contributing to the development of skincare products.
Used in Neurodegenerative Disease Treatment Research:
ISOQUINOLINE-1,3,4-TRIONE is used as a potential therapeutic agent in research for the treatment of neurodegenerative diseases, given its demonstrated neuroprotective properties.
Used in Sunscreen Products:
ISOQUINOLINE-1,3,4-TRIONE is used as a UV-absorbing component in sunscreen products, capitalizing on its ability to protect the skin from harmful ultraviolet radiation.
Further research is necessary to fully understand the potential benefits and risks of ISOQUINOLINE-1,3,4-TRIONE in these applications, ensuring its safe and effective use across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 521-73-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 521-73:
(5*5)+(4*2)+(3*1)+(2*7)+(1*3)=53
53 % 10 = 3
So 521-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO3/c11-7-5-3-1-2-4-6(5)8(12)10-9(7)13/h1-4H,(H,10,12,13)
521-73-3Relevant academic research and scientific papers
CYCLIC ACYLIMINES: I. SYNTHESIS AND REACTIVITY OF ISOQUINOLINE-1,4-DIONES
Alonso-Silva, Ignacio J.,Pardo, Mercedes,Soto, Jose L.
, p. 357 - 364 (2007/10/02)
3-Methoxycarbonylisoquinoline-1,4-dione (1) has been prepared through elimination processes from appropriate starting materials.The quinone was trapped by cycloaddition reactions with conjugated dienes.High regioselectivity was observed.A similar approach to prepare 3-benzoylisoquinoline-1,4-dione (2) was unsuccessful.
