85720-85-0 Usage
Uses
Used in Pharmaceutical Industry:
Phenyl 5,6,7,8-tetrahydro-1-hydroxy-2-naphthoate is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties. Its structural characteristics and potential therapeutic effects make it a candidate for drug development, particularly in the treatment of conditions that involve oxidative stress and inflammation.
Used in Drug Development:
Phenyl 5,6,7,8-tetrahydro-1-hydroxy-2-naphthoate is utilized in the development of new drugs due to its potential biological activities. Further studies are required to fully understand its pharmacological potential and explore its possible applications in treating various diseases and disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 85720-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,2 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85720-85:
(7*8)+(6*5)+(5*7)+(4*2)+(3*0)+(2*8)+(1*5)=150
150 % 10 = 0
So 85720-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O3/c18-16-14-9-5-4-6-12(14)10-11-15(16)17(19)20-13-7-2-1-3-8-13/h1-3,7-8,10-11,18H,4-6,9H2
85720-85-0Relevant academic research and scientific papers
Regioselective and Chemoselective Reduction of Naphthols Using Hydrosilane in Methanol: Synthesis of the 5,6,7,8-Tetrahydronaphthol Core
He, Yuan,Tang, Jinghua,Luo, Meiming,Zeng, Xiaoming
supporting information, p. 4159 - 4163 (2018/07/29)
A regioselective and chemoselective method for catalytic synthesis of biologically interesting 5,6,7,8-tetrahydronaphthols by reduction of naphthols was described. The side aromatic hydrocarbons in naphthols were site-selectively reduced, using hydrosilanes in methanol, allowing for retaining functional phenol scaffolds intact. It presents a rare example of using low-cost and air-stable hydrosilane for catalytic reduction of unactivated aromatic hydrocarbons under mild conditions. This reaction is scalable and proceeds in high selectivity without the formation of 1,2,3,4-tetrahydronaphthol byproducts with toleration of sensitive functionalities such as bromide, chloride, fluoride, ketone, ester, and amide.
