133406-89-0 Usage
Chemical composition
Consists of a benzene ring, a dihydroisoquinoline group, and an aniline group.
Usage
Commonly used in organic synthesis and pharmaceutical research.
Potential applications
Development of new drugs and as a building block for the synthesis of more complex organic molecules.
Suitability
Suitable for use as a ligand in metal-catalyzed reactions or as a substrate in organic transformations.
Unique features
Attractive to researchers due to its unique structure and potential utility in various chemical and biological contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 133406-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133406-89:
(8*1)+(7*3)+(6*3)+(5*4)+(4*0)+(3*6)+(2*8)+(1*9)=110
110 % 10 = 0
So 133406-89-0 is a valid CAS Registry Number.
133406-89-0Relevant academic research and scientific papers
CYCLIZATION OF N-(2-AMINOBENZYL) BENZYLAMINO-1-PHENYL-1-ETHANOLS AND DEBENZYLATION OF THE RESULTING TETRAHYDROISOQUINOLINE DERIVATIVES
Zara-Kaczian, Erzsebet,Deak, Gyula,Szoelloesy, Aron,Brlik, Janos
, p. 743 - 755 (2007/10/02)
Debenzylation reactions of 2-(o-aminobenzyl)-4-phenyl-1,2,3,4-tetrahydroisoquinolines (3a, b) and their N-acetyl derivatives (4a, b), obtained by the cyclization of N-(2-aminobenzyl)benzylamino-1-phenyl-1-ethanols (1), were studied.
