105950-92-3 Usage
Uses
Due to the limited information provided about the specific applications of 2-(chloromethyl)-4-(piperidin-1-yl)pyrimidine, it is challenging to list its uses accurately. However, based on its chemical structure and classification, it can be inferred that it may have potential applications in the following areas:
Used in Pharmaceutical Industry:
2-(chloromethyl)-4-(piperidin-1-yl)pyrimidine could be used as an intermediate or building block in the synthesis of various pharmaceutical compounds. Its unique structure, including the piperidine ring, may contribute to the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
As a pyrimidine derivative, 2-(chloromethyl)-4-(piperidin-1-yl)pyrimidine may be utilized in chemical research to explore its reactivity, stability, and potential interactions with other molecules. This could lead to a better understanding of its properties and possible applications in various fields.
Used in Material Science:
The aromatic nature of 2-(chloromethyl)-4-(piperidin-1-yl)pyrimidine and its heterocyclic structure may make it a candidate for use in the development of new materials with specific properties, such as conductivity, stability, or optical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 105950-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,5 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 105950-92:
(8*1)+(7*0)+(6*5)+(5*9)+(4*5)+(3*0)+(2*9)+(1*2)=123
123 % 10 = 3
So 105950-92-3 is a valid CAS Registry Number.
105950-92-3Relevant academic research and scientific papers
Pyrimidylalkylthio benzimidale compounds, pharmaceutical compositions and use
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, (2008/06/13)
This invention relates to 2- and 4-pyrimidinylmethylsulphinyl(and thio)benzimidazoles in which the pyrimidyl group is substituted by an optionally substituted amino group. These compounds inhibit exogenously and endogenously stimulated gastric acid secretion.
