741693-79-8 Usage
Description
2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol is a complex organic compound with a unique molecular structure. It is characterized by its pale brown solid appearance and is known to be a metabolite of the pharmaceutical drug Duloxetine. 2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol exhibits a range of chemical properties that make it potentially useful in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol is used as a metabolite for [application type] in the pharmaceutical industry. As a metabolite of Duloxetine, it plays a role in the drug's therapeutic effects and may be involved in the treatment of various medical conditions. 2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol's specific application reason in this context is to contribute to the overall efficacy and safety profile of Duloxetine as a medication.
Used in Chemical Research:
In the field of chemical research, 2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol is used as a subject of study for [application type] to better understand its chemical properties, reactivity, and potential applications. 2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol's unique structure and properties make it an interesting candidate for further investigation, which could lead to the development of new drugs, materials, or other products.
Used in Material Science:
2-Methoxy-5-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthalenol is used as a component in the development of new materials for [application reason] in the material science industry. Its chemical properties may offer unique advantages in the creation of advanced materials with specific characteristics, such as improved stability, reactivity, or other desirable traits.
Check Digit Verification of cas no
The CAS Registry Mumber 741693-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,6,9 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 741693-79:
(8*7)+(7*4)+(6*1)+(5*6)+(4*9)+(3*3)+(2*7)+(1*9)=188
188 % 10 = 8
So 741693-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO3S/c1-20-11-10-16(18-7-4-12-24-18)23-15-6-3-5-14-13(15)8-9-17(22-2)19(14)21/h3-9,12,16,20-21H,10-11H2,1-2H3/t16-/m0/s1
741693-79-8Relevant articles and documents
Synthesis and biological activity of some known and putative duloxetine metabolites
Kuo,Gillespie,Kulanthaivel,Lantz,Ma,Nelson,Threlkeld,Wheeler,Yi,Zmijewski
, p. 3481 - 3486 (2007/10/03)
Several putative phase I duloxetine metabolites, 4-hydroxy-, 5-hydroxy-, 6-hydroxy-, 5-hydroxy-6-methoxy-, 6-hydroxy-5-methoxy-, 5,6-dihydroxy-, and 4,6-dihydroxyduloxetine were synthesized, and their phase II metabolite as glucuronide or sulfate conjugates were also synthesized. Their in vitro binding activities were compared to that of parent compound duloxetine.
