1353946-17-4 Usage
Description
[1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine hydrochloride is a chemical compound derived from piperidine, featuring a pyrimidine moiety with a methoxy group. It is utilized in the research and pharmaceutical sectors, serving as an intermediate in the synthesis of various pharmaceuticals and organic compounds. [1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine hydrochloride has been investigated for its pharmacological properties and holds potential for the development of new drugs. The hydrochloride salt form enhances its solubility and stability in aqueous solutions, broadening its applicability within the pharmaceutical industry.
Uses
Used in Pharmaceutical Research and Development:
[1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine hydrochloride is used as a chemical intermediate for the synthesis of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable asset in the development of new drugs, contributing to the advancement of medical treatments.
Used in Drug Synthesis:
In the pharmaceutical industry, [1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine hydrochloride is used as a key component in the synthesis of drugs. Its presence in the molecular structure can influence the pharmacological properties of the final product, potentially leading to the creation of more effective medications.
Used in Solubility and Stability Enhancement:
The hydrochloride salt form of [1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine enhances the solubility and stability of the compound in aqueous solutions. This characteristic is particularly beneficial in the pharmaceutical industry, as it allows for easier formulation and administration of drugs, ultimately improving their efficacy and safety.
Used in Organic Chemistry:
[1-(6-Methoxy-pyriMidin-4-yl)-piperidin-4-yl]-Methyl-aMine hydrochloride also finds application in the field of organic chemistry, where it can be employed as a reagent or catalyst in various chemical reactions. Its unique structure and functional groups enable it to participate in a range of reactions, further expanding its utility in the synthesis of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1353946-17-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,9,4 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1353946-17:
(9*1)+(8*3)+(7*5)+(6*3)+(5*9)+(4*4)+(3*6)+(2*1)+(1*7)=174
174 % 10 = 4
So 1353946-17-4 is a valid CAS Registry Number.