52346-14-2 Usage
Uses
Used in Pharmaceutical Industry:
(4AS,8AS)-2-BENZOYL-1,3,4,4A,5,8A-HEXAHYDRO-6(2H)-ISOQUINOLINONE is used as a potential anti-inflammatory and analgesic agent for its pharmacological properties. It may help in the development of new drugs to treat inflammation and pain.
Used in Medicinal Chemistry:
(4AS,8AS)-2-BENZOYL-1,3,4,4A,5,8A-HEXAHYDRO-6(2H)-ISOQUINOLINONE serves as a valuable building block in the synthesis of various biologically active compounds. Its unique structure and properties make it a promising candidate for the development of novel therapeutic agents.
Used in Drug Discovery:
(4AS,8AS)-2-BENZOYL-1,3,4,4A,5,8A-HEXAHYDRO-6(2H)-ISOQUINOLINONE is utilized in drug discovery research to identify new lead compounds with potential therapeutic applications. Its versatile chemical properties allow for further modification and optimization to enhance its pharmacological effects.
Overall, (4AS,8AS)-2-BENZOYL-1,3,4,4A,5,8A-HEXAHYDRO-6(2H)-ISOQUINOLINONE is a promising chemical compound with potential applications in various fields, including pharmaceuticals, medicinal chemistry, and drug discovery. Its unique structure and properties make it a valuable asset in the development of new therapeutic agents and the advancement of scientific research.
Check Digit Verification of cas no
The CAS Registry Mumber 52346-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,4 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52346-14:
(7*5)+(6*2)+(5*3)+(4*4)+(3*6)+(2*1)+(1*4)=102
102 % 10 = 2
So 52346-14-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO2/c18-15-7-6-14-11-17(9-8-13(14)10-15)16(19)12-4-2-1-3-5-12/h1-7,13-14H,8-11H2/t13-,14-/m0/s1
52346-14-2Relevant academic research and scientific papers
A novel, stereoselective synthesis of cis-4a(S), 8a(R)-decahydro-6(2H)-isoquinolones from meroquinene esters
Martinelli,Peterson,Khau,Hutchison,Sullivan
, p. 5413 - 5416 (2007/10/02)
Intramolecular cyclization of N-acylated meroquinene t-butyl esters in cold H2SO4 cleanly afforded cis-4a(S), 8a(R)-decahydro-6(2H)-isoquinolones with complete stereocontrol in >95% yield. Formation of the meroquinene esters from cinchona alkaloid autoxidation using an improved Doering protocol was accomplished in three steps with 85% overall yield.
