138614-32-1 Usage
Description
(R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE is a chemical compound belonging to the class of arylalkylamines. It is a hydrochloride salt of the amine compound, which enhances its stability and ease of handling. (R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE is characterized by its unique structure, which includes a phenyl group, a trifluoromethyl-phenoxy group, and a propylamine chain, endowing it with distinct properties and potential pharmaceutical applications. As a hydrochloride salt, it exhibits improved water solubility and potentially enhanced bioavailability compared to its non-salt form. (R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE is a versatile compound with a wide range of scientific and medical applications.
Uses
Used in Pharmaceutical Research and Development:
(R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE is used as a research compound for its potential applications in the field of pharmacology and medicinal chemistry. Its unique structure and properties make it a valuable tool for exploring new drug candidates and therapeutic strategies.
Used in Drug Synthesis:
In the pharmaceutical industry, (R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE is used as a key intermediate in the synthesis of various drugs. Its versatile structure allows for the development of new compounds with specific therapeutic targets and improved pharmacological profiles.
Used in Drug Delivery Systems:
(R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE can be employed in the development of novel drug delivery systems, aiming to enhance the bioavailability, targeting, and overall efficacy of pharmaceutical agents. Its hydrochloride salt form may facilitate improved solubility and stability, which are crucial factors in drug delivery.
Used in Chemical Research:
(R)-3-PHENYL-3-(4-TRIFLUOROMETHYL-PHENOXY)-PROPYLAMINE HYDROCHLORIDE serves as a valuable compound in chemical research, particularly in the study of arylalkylamines and their derivatives. Its unique structure allows for the investigation of various chemical reactions and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 138614-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138614-32:
(8*1)+(7*3)+(6*8)+(5*6)+(4*1)+(3*4)+(2*3)+(1*2)=131
131 % 10 = 1
So 138614-32-1 is a valid CAS Registry Number.
138614-32-1Relevant articles and documents
A convenient method for preparing enantiomerically pure norfluoxetine, fluoxetine and tomoxetine
Koenig, Thomas M.,Mitchell, David
, p. 1339 - 1342 (2007/10/02)
A convenient synthesis for enantiomers of norfluoxetine, fluoxetine and tomoxetine is described. All final products were derived from a common intermediate, 3-phenyl-3-hydroxypropylamine.
