554-92-7 Usage
Description
Trimethobenzamide Hydrochloride is a pharmaceutical compound with antiemetic properties, which means it is used to prevent nausea and vomiting. It is also utilized in the treatment of Parkinson's disease, where it helps alleviate some of the symptoms associated with the condition.
Uses
Used in Pharmaceutical Industry:
Trimethobenzamide Hydrochloride is used as an antiemetic agent for the prevention of nausea and vomiting in patients. It is particularly effective in managing these symptoms, which can be caused by various factors such as motion sickness, chemotherapy, or postoperative recovery.
Used in Parkinson's Disease Treatment:
In the treatment of Parkinson's disease, Trimethobenzamide Hydrochloride is used to alleviate some of the symptoms associated with the condition. It helps improve the patient's quality of life by reducing the severity of symptoms such as tremors, rigidity, and bradykinesia.
Therapeutic Function
Antinauseant
Check Digit Verification of cas no
The CAS Registry Mumber 554-92-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 554-92:
(5*5)+(4*5)+(3*4)+(2*9)+(1*2)=77
77 % 10 = 7
So 554-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H28N2O5.ClH/c1-23(2)10-11-28-17-8-6-15(7-9-17)14-22-21(24)16-12-18(25-3)20(27-5)19(13-16)26-4;/h6-9,12-13H,10-11,14H2,1-5H3,(H,22,24);1H
554-92-7Relevant articles and documents
An improved process for trimethobenzamide hydrochloride
Neelakandan,Manikandan,Santosha,Prabhakaran
, p. 981 - 984 (2013/08/23)
An improved process for the preparation of trimethobenzamide hydrochloride conforming to regulatory specification is reported. Specifically, a process for the preparation of trimethobenzamide hydrochloride, which is free from the associated impurities that are normally encountered during coupling of 4-(2-dimethylaminoethoxy)benzyl amine with 3,4,5-trimethoxy benzoic acid is described.
