54767-74-7 Usage
Description
(R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride, with the molecular formula C23H39NO2S?HCl, is a hydrochloride salt that belongs to the class of organic compounds known as phenylamino-alkyl-benzenes. (R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride is characterized by its isopropylthio and octylaminoethyl substituents attached to a benzyl alcohol backbone, which contributes to its unique chemical properties and potential applications.
Uses
Used in Pharmaceutical Research:
(R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride is used as a selective alpha 2C-adrenergic receptor antagonist for pharmaceutical research. Its application is based on its ability to selectively bind to and block the action of certain adrenergic receptors, which can be beneficial in the treatment of various conditions.
Used in the Treatment of Hypertension:
In the medical field, (R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride is used as a therapeutic agent for the treatment of hypertension. Its application is due to its potential to modulate the adrenergic system, which plays a role in regulating blood pressure.
Used in Chronic Pain Management:
(R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride is also used in the management of chronic pain. Its application is based on the hypothesis that its interaction with adrenergic receptors may help alleviate pain signals in the body.
Used in Anxiety Treatment:
(R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride has potential applications in the treatment of anxiety disorders. Its use is supported by the idea that its antagonistic action on specific adrenergic receptors may help reduce anxiety symptoms.
Used in Synthetic Organic Chemistry:
In the field of synthetic organic chemistry, (R,R)-4-[isopropylthio]-alpha-[1-(octylamino)ethyl]benzyl alcohol hydrochloride may serve as a building block for the development of new drugs or therapeutic agents. Its application is due to its unique structural features, which can be exploited in the synthesis of novel compounds with potential medicinal properties.
Check Digit Verification of cas no
The CAS Registry Mumber 54767-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,6 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54767-74:
(7*5)+(6*4)+(5*7)+(4*6)+(3*7)+(2*7)+(1*4)=157
157 % 10 = 7
So 54767-74-7 is a valid CAS Registry Number.
54767-74-7Relevant articles and documents
Alkyl and cycloalkylthiophenylalkylaminoalkanols, their salts and the preparation thereof
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, (2008/06/13)
Amino-alcohols of the formula STR1 wherein R1 represents either a linear or branched chain alkyl radical having 1 to 4 carbon atoms, or a cycloalkyl radical having 5 or 6 carbon atoms; R2 represents a lower alkyl radical having 1 or 2 carbon atoms; R3 represents a linear or branched chain alkyl radical having 3 to 10 carbon atoms which radical is optionally substituted by phenyl; R4 represents hydrogen, or, together with R3 and the adjacent nitrogen atom, a heterocyclic nucleus of the piperidine type and the corresponding non-toxic salts of said amino-alcohols; preparation of the above and their use as antispasmodic, peripheral vasodilatory and anti-hypertensive agents and as an agent having a protective activity against anoxia of the myocardium.
