21040-59-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6-methoxy-2-methylisoquinolin-7-ol is used as a potential pharmaceutical candidate for [application reason] due to its unique molecular structure and chiral configuration. (S)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6-methoxy-2-methylisoquinolin-7-ol's potential pharmacological or biological activity makes it a promising substance for further research and development in the pharmaceutical field.
Used in Chemical Research:
In the field of chemical research, (S)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6-methoxy-2-methylisoquinolin-7-ol serves as a subject for studying the effects of its molecular structure and chirality on its properties and reactivity. This research could lead to a better understanding of similar compounds and their potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 21040-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,4 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21040-59:
(7*2)+(6*1)+(5*0)+(4*4)+(3*0)+(2*5)+(1*9)=55
55 % 10 = 5
So 21040-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H25NO4/c1-21-8-7-14-11-19(24-3)17(22)12-15(14)16(21)9-13-5-6-18(23-2)20(10-13)25-4/h5-6,10-12,16,22H,7-9H2,1-4H3/t16-/m0/s1
21040-59-5Relevant academic research and scientific papers
Enzymatic resolution of acylates of prochiral phenolic 1-aryl- and 1-arylalkyl-1,2,3,4-tetrahydroisoquinolinols, which possess a Guaiacol-type moiety, by use of immobilized lipase in organic solvent
Hoshino,Tanahashi,Okada,Akita,Oishi
, p. 933 - 942 (2007/10/02)
Enzymatic resolution of acylates of prochiral phenolic 1-aryl, and 1-arylalkyl-1,2,3,4-tetrahydroisoquinolinols, which possess a guaiacol-type moiety by use of lipase immobilized with celite in water-saturated organic solvent gave the corresponding acylates and phenols in moderate optical yields.
