5934-50-9 Usage
Uses
Used in Gastrointestinal Disorders Treatment:
Hyoscyamine hydrochloride is used as a therapeutic agent for treating gastrointestinal disorders such as irritable bowel syndrome, diverticulitis, and peptic ulcer disease. By inhibiting the effects of acetylcholine, it helps to alleviate symptoms like abdominal pain, cramping, and bloating, providing relief to patients suffering from these conditions.
Used in Pharmaceutical Formulations:
Available in various forms such as tablets, capsules, and oral solutions, hyoscyamine hydrochloride is used as an active pharmaceutical ingredient in different dosage forms. It is typically prescribed to be taken multiple times a day, as directed by healthcare professionals, to ensure optimal therapeutic effects.
Used in Symptom Relief:
Hyoscyamine hydrochloride serves as a symptom-relief medication, reducing the discomfort associated with gastrointestinal motility issues. Its ability to decrease gastrointestinal motility helps in managing symptoms effectively, improving the quality of life for patients with gastrointestinal disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 5934-50-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5934-50:
(6*5)+(5*9)+(4*3)+(3*4)+(2*5)+(1*0)=109
109 % 10 = 9
So 5934-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO3.ClH/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12;/h2-6,13-16,19H,7-11H2,1H3;1H/t13?,14?,15?,16-;/m1./s1
5934-50-9Relevant academic research and scientific papers
Stereochemistry of the 1,2-migration of the carboxyl group that occurs during the biosynthesis of tropic acid from phenylalanine
Leete, Edward
, p. 226 - 228 (2007/10/02)
(2S,3R)- and (2S,3S)-phenylalanine were fed in separate experiments to Datura innoxia plants.The distribution of isotopes in the resultant labeled hyoscyamine and scopolamine indicates that the biosynthesis of the acid moiety of these ester alkaloids, namely (S)-tropic acid, involves the migration of the carboxyl group of phenylalanine to its prochiral C-3 position with retention of configuration.
