171897-38-4 Usage
Uses
Used in Pharmaceutical Industry:
Pregabalin is used as a medication for treating nerve pain, seizures, and anxiety disorders. It is effective in managing these conditions due to its ability to slow down brain impulses that cause seizures and its influence on brain chemicals responsible for pain signals.
Used in Neurological Treatments:
As an anticonvulsant, pregabalin is used for the treatment of various neurological conditions, including epilepsy and neuropathic pain. It helps in reducing the frequency and severity of seizures and provides relief from nerve pain associated with conditions like diabetic peripheral neuropathy and postherpetic neuralgia.
Used in Psychiatric Treatments:
Pregabalin is also utilized in psychiatric treatments for generalized anxiety disorder and other anxiety-related conditions. It helps in alleviating anxiety symptoms by modulating the brain's chemical responses.
Common side effects of pregabalin may include dizziness, drowsiness, weight gain, and difficulty concentrating. It is crucial to adhere to the prescribed dosage and usage instructions provided by a healthcare professional when using pregabalin to ensure its safety and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 171897-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,9 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 171897-38:
(8*1)+(7*7)+(6*1)+(5*8)+(4*9)+(3*7)+(2*3)+(1*8)=174
174 % 10 = 4
So 171897-38-4 is a valid CAS Registry Number.
171897-38-4Relevant academic research and scientific papers
Stereospecific synthesis of (R)- and (S)-Baclofen and (R)- and (S)- PCPGABA [4-amino-2-(4-chlorophenyl)butyric acid] via (R)- and (S)-3-(4- chlorophenyl)pyrrolidines
Yoshifuji,Kaname
, p. 1302 - 1306 (2007/10/02)
(R)- and (S)-baclofen and (R)- and (S)-PCPGABA [4-amino-2-(4- chlorophenyl)butyric acid] were stereospecifically synthesized via (R)- and (S)-3-(4-chlorophenyl)pyrrolidines, starting from trans-4-hydroxy-L-proline. The syntheses involve two key operations
