1391054-22-0 Usage
Description
4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide is a complex organic compound with a unique chemical structure. It is characterized by its molecular composition, which includes an amino group, a pyrrolidinylmethyl group, a methyl group, an ethylsulfonyl group, and a methoxybenzamide group. 4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide has potential applications in various fields due to its specific chemical properties and interactions.
Uses
Used in Pharmaceutical Industry:
4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide is used as an active pharmaceutical ingredient (API) for the development of new drugs. Its unique chemical structure allows it to interact with specific biological targets, making it a promising candidate for the treatment of various medical conditions.
Used in Chemical Research:
In the field of chemical research, 4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique functional groups and reactivity make it a valuable tool for exploring new chemical reactions and developing novel synthetic pathways.
Used in Material Science:
4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide may also find applications in material science, particularly in the development of new polymers or other advanced materials. Its specific chemical properties, such as its ability to form hydrogen bonds or interact with other molecules, could be exploited to create materials with unique properties or improved performance.
Used in Analytical Chemistry:
4-amino-N-[(1-ethyl-2-pyrrolidinyl)methyl]-N-[methyl]-5-(ethylsulfonyl)-2-methoxybenzamide can be employed as a reference material or standard in analytical chemistry, particularly in the development and validation of new analytical methods or techniques. Its unique chemical structure and properties make it a valuable tool for testing and optimizing the performance of analytical instruments and methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1391054-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,0,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1391054-22:
(9*1)+(8*3)+(7*9)+(6*1)+(5*0)+(4*5)+(3*4)+(2*2)+(1*2)=140
140 % 10 = 0
So 1391054-22-0 is a valid CAS Registry Number.
1391054-22-0Relevant articles and documents
Synthesis method of process impurity of amisulpride
-
Paragraph 0012-0013, (2021/07/09)
The invention discloses a synthesis method of a process impurity of amisulpride, and belongs to the technical field of chemical pharmacy. N-ethyl-2-aminomethylpyrrolidine (2) reacts with (BOC)2O to obtain 1-ethyl pyrrolidine-2-methyl tert-butyl carbamate (3); CH3I is added under the alkaline condition of NaH, and methylation is performed to obtain N-(1-ethyl pyrrolidine-2-methyl), N-methyl tert-Butyl carbamate (4); under an acidic condition, hydrolysis is carried out to obtain N-ethyl-2-methylaminomethylpyrrolidine (5); and finally reaction with 4-amino-5-(ethylsulfonyl)-2-methoxybenzoic acid (6) is performed under the catalysis of theorganic alkali N',N-carbonyldiimidazole (CDI) to obtain an amisulpride impurity (1). The synthesized high-purity amisulpride impurity is used as an impurity standard substance in detection and analysis ofamisulpride finished products, so that the positioning accuracy of the amisulpride impurity is improved; control on impurities is enhanced, and the purpose of controlling the quality of the finished amisulpride is finally achieved; and the raw materials are simple and easy to obtain, and operation is simple.
