41450-85-5 Usage
Uses
Used in Neuroprotective Applications:
Harman is used as a neuroprotective agent for its potential to protect neurons from damage and degeneration, which may be beneficial in the treatment of neurological disorders.
Used in Antioxidant Applications:
As an antioxidant, Harman is utilized to neutralize harmful free radicals and reduce oxidative stress, which can contribute to various diseases and aging processes.
Used in Cancer Treatment Research:
Harman is investigated as a potential anti-cancer agent, with studies exploring its ability to inhibit cancer cell growth and induce apoptosis in certain types of cancer.
Used in Understanding Hallucinogenic Mechanisms:
Due to its psychoactive properties, Harman serves as a tool for researchers to study the mechanisms of hallucinogenic drugs, potentially leading to advancements in the development of novel therapeutic agents for mental health disorders.
Used in Traditional Medicine and Shamanic Practices:
Harman has been employed in traditional medicine and shamanic practices for its psychoactive effects, although its use in these contexts requires careful consideration due to potential toxicity and side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 41450-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,5 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41450-85:
(7*4)+(6*1)+(5*4)+(4*5)+(3*0)+(2*8)+(1*5)=95
95 % 10 = 5
So 41450-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2/c1-8-11(2,3)9-6-5-7-12-10(9)13(8)4/h5-7H,1H2,2-4H3
41450-85-5Relevant academic research and scientific papers
Red colouring photochromic 6′-substituted spiroindolinonaphth[2,1-b][1,4]oxazines
Rickwood,Marsden,Ormsby,Staunton,Wood,Hepworth,Gabbutt
, p. 17 - 24 (2007/10/02)
Electron donating/withdrawing substituents and electronegative centres have been successfully employed in substantially widening the range of photo-generated colours available in the spiroindolinonaphthoxazine class of photochromic materials.
