28519-59-7 Usage
Type of compound
Heterocyclic compound
Central structure
Isoindole ring
Attached groups
Two phenyl groups
Applications
Organic synthesis and pharmaceutical research
Therapeutic properties
Potential GABA-A receptor modulator
Potential treatment
Neurological disorders
Additional properties
Antibacterial and antifungal properties
Versatility
Potential applications in various fields
Check Digit Verification of cas no
The CAS Registry Mumber 28519-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,1 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28519-59:
(7*2)+(6*8)+(5*5)+(4*1)+(3*9)+(2*5)+(1*9)=137
137 % 10 = 7
So 28519-59-7 is a valid CAS Registry Number.
28519-59-7Relevant academic research and scientific papers
Schiff Bases as External and Internal Electrophiles in Reactions of Functionalized Organolithium Reagents. A New Route to Isoindoline Derivatives and 1,2,3,4-Tetrahydroisoquinolines
Bradsher, Charles K.,Hunt, David A.
, p. 327 - 330 (2007/10/02)
Reaction of Schiff bases with certain functionalized organolithium reagents is useful in the synthesis of 1,2-diarylisoindolines and 2,3-diarylphthalimidines.Schiff bases derived from 2-(2-bromophenyl)ethylamines on halogen-metal exchange with butyllithium undergo a Parham-type cyclization to yield 1-aryl-1,2,3,4-tetrahydroisoquinolines.
