187456-97-9 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-propyl-, methyl ester is used as a muscle relaxant and anticonvulsant for the treatment of various conditions. It is particularly effective in managing cerebral palsy, muscle spasticity, and multiple sclerosis due to its ability to regulate GABA levels in the brain, thus providing relief from muscle spasms and stiffness.
Used in Medical Treatment:
Ethopropazine is utilized in medical treatment to alleviate the symptoms of muscle-related conditions. It is prescribed by healthcare professionals in oral tablet form, and its administration should be strictly followed to minimize the risk of side effects. 1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-2-propyl-, methyl ester's role in modifying GABA levels makes it a valuable asset in the management of muscle spasms and stiffness, contributing to the improvement of the patient's quality of life.
Check Digit Verification of cas no
The CAS Registry Mumber 187456-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,4,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 187456-97:
(8*1)+(7*8)+(6*7)+(5*4)+(4*5)+(3*6)+(2*9)+(1*7)=189
189 % 10 = 9
So 187456-97-9 is a valid CAS Registry Number.
187456-97-9Relevant academic research and scientific papers
Synthesis of β-hydroxypiperidine alkaloids by anodic oxidation of carbamates and hydroboration
Plehiers, Mark,Hootelé, Claude
, p. 2444 - 2453 (2007/10/03)
The β-hydroxypiperidine alkaloids (±)-pseudoconhydrine, (±)-N-methylpseudoconhydrine, (-)-5-hydroxysedamine, and (+)-sedacryptine were synthesized. Successive functionalization of the piperidine ring via anodic methoxylation allowed the regio- and stereos
Hydroboration of Enecarbamates and the Synthesis of β-Hydroxypiperidine Alkaloids
Plehiers, Mark,Hootele, Claude
, p. 7569 - 7570 (2007/10/02)
The β-hydroxypiperidine alkaloids 5, 6 and 8 were diastereoselectively synthesized using hydroboration of enecarbamates 2b-c as a key step.
