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(S)-2-Isopropylpyrrolidine hydrochloride, also known as baclofen hydrochloride, is a chemical compound that functions as a muscle relaxant and antispastic agent. It is a derivative of the neurotransmitter gamma-aminobutyric acid (GABA) and is classified as a GABAergic medication. (S)-2-Isopropylpyrrolidine hydrochloride works by influencing the nerves in the spinal cord that control muscle movement, making it a valuable treatment for various muscle-related conditions.

51207-71-7

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51207-71-7 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-Isopropylpyrrolidine hydrochloride is used as a muscle relaxant and antispastic agent for the treatment of muscle symptoms caused by conditions such as multiple sclerosis, spinal cord injuries, or other disorders. Its action on the nerves in the spinal cord helps alleviate spasticity and muscle spasms, providing relief to patients suffering from these conditions.
Used in Neurological Treatments:
As a GABAergic medication, (S)-2-Isopropylpyrrolidine hydrochloride is utilized in the management of neurological disorders that involve muscle stiffness and spasms. Its influence on the GABAergic system contributes to its effectiveness in treating these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 51207-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51207-71:
(7*5)+(6*1)+(5*2)+(4*0)+(3*7)+(2*7)+(1*1)=87
87 % 10 = 7
So 51207-71-7 is a valid CAS Registry Number.

51207-71-7Downstream Products

51207-71-7Relevant academic research and scientific papers

Intramolecular redox-triggered C-H functionalization

Jurberg, Igor D.,Peng, Bo,Woestefeld, Eckhard,Wasserloos, Maximilian,Maulide, Nuno

supporting information; experimental part, p. 1950 - 1953 (2012/04/04)

Sacrifice for the team: A one-pot method achieves remote functionalization at the α-position of an amine moiety through the sacrificial reduction of a neighboring group. The process takes advantage of an intramolecular redox reaction, thereby avoiding the need for any external oxidants. This method was applied to a concise five-step total synthesis of indolizidine 167B.

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