125159-93-5 Usage
Tosylate derivative
2-tosyl-2,3-dihydroisoquinolin-4(1H)-one is derived from 2,3-dihydroisoquinolin-4(1H)-one by the addition of a tosyl group (a sulfonamide group attached to a benzene ring).
High reactivity
This chemical compound is known for its high reactivity, making it a popular choice in organic synthesis and the preparation of various pharmaceuticals, agrochemicals, and other organic compounds.
Versatile building block
The unique structure and reactivity of 2-tosyl-2,3-dihydroisoquinolin-4(1H)-one make it a valuable and versatile building block for the synthesis of complex organic molecules.
Potential drug scaffold
Research has shown that 2-tosyl-2,3-dihydroisoquinolin-4(1H)-one has potential as a drug scaffold, indicating its possible use in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 125159-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,5 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 125159-93:
(8*1)+(7*2)+(6*5)+(5*1)+(4*5)+(3*9)+(2*9)+(1*3)=125
125 % 10 = 5
So 125159-93-5 is a valid CAS Registry Number.
125159-93-5Relevant academic research and scientific papers
BENZOPHENANTHRIDINES. VIII. SYNTHESIS AND STRUCTURE OF cis-2-METHOXY-5-TOSYL-4b,5,6,10b,11,12-HEXAHYDROBENZOPHENANTHRIDINE
Rozhkov, V. S.,Sladkov, V. I.,Turdybekov, K. M.,Lindeman, S. V.,Kolesnikov, A. Yu.,et al.
, p. 1162 - 1167 (2007/10/02)
The total synthesis of cis-2-methoxy-5-tosyl-4b,5,6,10b,11,12-hexahydrobenzophenathridine was realized from the hydrochloride of methyl aminoacetate by successive ring growth AB->ABD->ABDC in five stages, including the addition of 3-methoxyphenylmagnes
