106271-65-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Pyridineacetamide, N-methyl-(6CI,9CI) is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic effects. Its unique structure allows for the creation of molecules with specific binding affinities and biological activities, making it valuable in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Pyridineacetamide, N-methyl-(6CI,9CI) is utilized as a precursor in the production of pesticides and other agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases, thereby contributing to increased crop yields and protection of agricultural resources.
Used in Materials Science:
3-Pyridineacetamide, N-methyl-(6CI,9CI) also finds applications in materials science, where it can be used to develop new materials with specific properties. Its unique chemical structure allows for the creation of materials with tailored characteristics, such as improved conductivity, stability, or reactivity, which can be beneficial in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 106271-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106271-65:
(8*1)+(7*0)+(6*6)+(5*2)+(4*7)+(3*1)+(2*6)+(1*5)=102
102 % 10 = 2
So 106271-65-2 is a valid CAS Registry Number.
106271-65-2Relevant academic research and scientific papers
Nucleophilic Addition of 2-, 3-, or 4-pyridine to the Aziridine, 7-Methyl-7-azabicycloheptane
Rees, David C
, p. 147 - 150 (2007/10/02)
The synthesis of trans-(+/-)-N-methyl-N-amino>cyclohexyl>-4-benzofuranacetamide dihydrochloride, 1 which is a 3-pyridyl derivative of the kappa opioid analgesic trans-(+/-)-N-methyl-N-benzofuran-4-acetamide monohydrochloride, 2 is described.The key intermediate is trans-(+/-)-N,N'-dimethyl-N--1,2-cyclohexanediamine, 9 which is formed by nucleophilic addition of 3-pyridine 6 to the aziridine, 7-methyl-7-azabicycloheptane, 4.During attempts to prepare the 2- or 4-isomeric pyridyl derivatives of 1 it was discovered that both 2- or 4-pyridine, 5 or 7 are converted to N-methyl-N,N-di- 11 and N-methyl-N,N-di 13 respectively by refluxing in toluene in the presence of ammonium chloride.The 3-isomer, 6 is unchanged after treatment under identical conditions.Careful control of the reaction conditions enabled the aziridine 4 to be ring opened with the pyridyl amines 5 or 7 to give the 1,2-diamines trans-(+/-)-N,N'-dimethyl-N--1,2-cyclohexanediamine, 8 or trans-(+/-)-N,N'-dimethyl-N--1,2-cyclohexane diamine 10 respectively.
