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[R-(R,S)]-alpha-[1-(benzylamino)ethyl]benzyl alcohol hydrochloride is a chemical compound that belongs to the class of alpha-agonist adrenergic receptors. It is a hydrochloride salt derivative of the alpha-1 adrenergic receptor agonist, known for its ability to stimulate these receptors, leading to vasoconstriction and increased blood pressure.

61347-75-9

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61347-75-9 Usage

Uses

Used in Medical Applications:
[R-(R,S)]-alpha-[1-(benzylamino)ethyl]benzyl alcohol hydrochloride is used as a sympathomimetic and vasopressor drug for the treatment of hypotension, shock, and low blood pressure during anesthesia. It acts by stimulating the alpha-1 adrenergic receptors, which results in vasoconstriction and increased blood pressure, making it a valuable tool in managing these conditions.
Used in Cardiology:
In the field of cardiology, [R-(R,S)]-alpha-[1-(benzylamino)ethyl]benzyl alcohol hydrochloride is used as a treatment for certain types of heart failure and septic shock. Its ability to increase blood pressure and improve circulation can be beneficial in these critical situations, providing support to patients who are experiencing these life-threatening conditions.
Used in Anesthesiology:
During surgical procedures, [R-(R,S)]-alpha-[1-(benzylamino)ethyl]benzyl alcohol hydrochloride is used as a vasopressor to manage low blood pressure that may occur during anesthesia. Its rapid onset and short duration of action make it an ideal choice for maintaining hemodynamic stability during surgery.

Check Digit Verification of cas no

The CAS Registry Mumber 61347-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61347-75:
(7*6)+(6*1)+(5*3)+(4*4)+(3*7)+(2*7)+(1*5)=119
119 % 10 = 9
So 61347-75-9 is a valid CAS Registry Number.

61347-75-9Downstream Products

61347-75-9Relevant academic research and scientific papers

Transimination. Conversion of Nitriles into Secondary Amines in a One-Pot Reaction.

Brussee, J.,Gen, A. van der

, p. 25 - 26 (2007/10/02)

Transimination has been used as a key step into convenient, highly erythro selective, one-pot synthesis of N-substituted β-ethanolamines from (R)-(+)--benzeneacetonitrile (OTBS-mandelonitrile).

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