51424-33-0 Usage
Description
(1R)-6-hydroxy-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium chloride is a complex tetrahydroisoquinolinium derivative featuring a hydroxy group at the 6th position, a methoxy group at the 7th position, and a methyl group at the 1st position. This chemical compound also includes a quaternary ammonium group and a chloride ion, which may contribute to its potential pharmacological or biological activities. Its unique structure suggests that further research is necessary to explore its possible applications.
Uses
Used in Pharmaceutical Industry:
(1R)-6-hydroxy-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium chloride is used as a potential pharmaceutical candidate for [specific application reason, if known] due to its unique chemical structure and the presence of functional groups that may interact with biological targets.
Used in Research and Development:
In the field of scientific research, (1R)-6-hydroxy-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium chloride serves as a subject of study for exploring its pharmacological properties and potential biological activities, with the aim of identifying new therapeutic agents or understanding its mechanisms of action.
Please note that without specific details on the applications or reasons for using (1R)-6-hydroxy-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium chloride, the uses listed are general and based on the assumption that its unique structure may have pharmacological relevance. Further research would be required to pinpoint exact applications and reasons.
Check Digit Verification of cas no
The CAS Registry Mumber 51424-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,2 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51424-33:
(7*5)+(6*1)+(5*4)+(4*2)+(3*4)+(2*3)+(1*3)=90
90 % 10 = 0
So 51424-33-0 is a valid CAS Registry Number.
51424-33-0Relevant articles and documents
Study of chiral β-enaminones prepared from pyrrolidine, cytisine, salsoline and 2-amino-1-(4-nitrophenyl)propane-1,3-diol: Resolution of salsoline via diastereomeric modified carane-type β-enaminones
Popov, Sergey A.,Gatilov, Yuri V.,Rybalova, Tatjana V.,Tkachev, Alexey V.
, p. 233 - 238 (2003)
A series of novel optically active β-enaminones have been prepared regio- and stereoselectively from primary and secondary amines (pyrrolidine, cytisine salsoline and 2-amino-1-(4-nitrophenyl)propane-1,3-diol) and (+)-3-carene-derived β-chlorovinylketone. Resolution of the isoquinoline alkaloid salsoline has been demonstrated as well as isolation of a single diastereomeric adduct from racemic 2-amino-1-(4-nitrophenyl)propane-1,3-diol.
