22005-25-0 Usage
Compound class
Isoindoles
Redox-active
Capable of undergoing redox reactions
Antioxidant
Presence of hydroxyphenyl group provides antioxidant properties
Organic electronics
Utilizing its redox-active properties
Pharmaceutical agent
Showing potential as a neuroprotective and anti-inflammatory agent in preclinical studies
Electrochemical sensors
Due to its ability to undergo redox reactions
Energy storage devices
Also attributed to its redox-active nature
Current status
Research is ongoing, with potential for various practical and medical applications in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 22005-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,0 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22005-25:
(7*2)+(6*2)+(5*0)+(4*0)+(3*5)+(2*2)+(1*5)=50
50 % 10 = 0
So 22005-25-0 is a valid CAS Registry Number.
22005-25-0Relevant academic research and scientific papers
Synthesis and characterization of new aromatic hydroxy acid compounds
Thiruvasagam
, p. 523 - 530 (2018/12/13)
Four novel aromatic hydroxy acid (HA) compounds N-(4-hydroxyphenyl)-4’-trimellitimide, N-(3-hydroxyphenyl)-4’-trimellitimide, N-(5-hydroxynaphthyl)-4’-trimellitimide and N-{4’-[2-(4-hydroxyphenyl) isopropyl phenyl]}-4’’-trimellitimide are synthesized thro
Design, synthesis, and structure-activity relationships of phthalimide- phenylpiperazines: A novel series of potent and selective {1a)-adrenergic receptor antagonists
Kuo, Gee-Hong,Prouty, Catherine,Murray, William V.,Pulito, Virginia,Jolliffe, Linda,Cheung, Peter,Varga, Sally,Evangelisto, Mary,Wang, Jian
, p. 2183 - 2195 (2007/10/03)
Beginning from the screening hit and literature α1-adrenergic compounds, a hybridized basic skeleton A was proposed as the pharmacophore for potent and selective α(1a)-AR antagonists. Introduction of a hydroxy group to increase the flexibility
