85720-85-0 Usage
General Description
Phenyl 5,6,7,8-tetrahydro-1-hydroxy-2-naphthoate is a chemical compound that belongs to the class of esters. It is derived from naphthalene and has a hydroxy group attached to the tetrahydrophenyl ring. Phenyl 5,6,7,8-tetrahydro-1-hydroxy-2-naphthoate possesses potential biological activities, including antioxidant and anti-inflammatory properties. It may have applications in the field of pharmacology and drug development due to its structural characteristics and potential therapeutic effects. Further studies are needed to fully understand the pharmacological potential and possible uses of Phenyl 5,6,7,8-tetrahydro-1-hydroxy-2-naphthoate.
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 articles and documents
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.
