122913-68-2 Usage
Properties
1. Chemical Structure: It is derived from naphthalene with a hydroxy group and an acetate group attached to the 1,2,3,4-tetrahydro-1-naphthyl ring.
2. Functional Groups: Contains a hydroxy group (-OH) and an acetate group (-COOCH3).
3. Potential Medicinal Applications: Studied for potential medicinal and pharmacological uses.
4. Pharmacological Properties: Investigated for serotonin receptor agonism, anti-inflammatory, and antioxidant effects.
Specific Content
1. Serotonin Receptor Agonist:
Potential to act as a serotonin receptor agonist.
Implications for the treatment of neurological and psychiatric disorders.
2. Anti-inflammatory Properties:
Investigated for potential anti-inflammatory effects.
3. Antioxidant Properties:
Studied for potential antioxidant properties.
4. Research Status:
Further research needed to fully understand pharmacological effects and applications.
5-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl acetate shows promise in various areas of medicine and pharmacology, but more research is required to confirm its therapeutic potential and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 122913-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,1 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 122913-68:
(8*1)+(7*2)+(6*2)+(5*9)+(4*1)+(3*3)+(2*6)+(1*8)=112
112 % 10 = 2
So 122913-68-2 is a valid CAS Registry Number.
122913-68-2Relevant academic research and scientific papers
Regio- and Chemo-selective Properties of Lipase from Candida cylindracea
Pedrocchi-Fantoni, Giuseppe,Servi, Stefano
, p. 1029 - 1034 (2007/10/02)
Lipase from Candida cylindracea allows discrimination between the two connectively non-equivalent hydroxy groups in primary diols or their esters via acylation-hydrolysis, with high regioselectivity.The same technique is used to distinguish between hydroxy groups of different nature in phenolic compounds.
