15231-63-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Pyrimidinamine, N,4-dimethyl(9CI) is utilized as an intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting various diseases and conditions.
Used in Agrochemical Production:
In addition to its pharmaceutical applications, 2-Pyrimidinamine, N,4-dimethyl(9CI) is also used in the production of agrochemicals. Its properties make it suitable for the creation of compounds that can be used in agriculture to improve crop yields and protect plants from pests and diseases.
Used in Organic Chemistry Research:
2-Pyrimidinamine, N,4-dimethyl(9CI) holds potential applications in the field of organic chemistry, where it can be employed as a research compound. Its unique structure and properties make it valuable for studying various chemical reactions and processes, contributing to the advancement of organic chemistry knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 15231-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,3 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15231-63:
(7*1)+(6*5)+(5*2)+(4*3)+(3*1)+(2*6)+(1*3)=77
77 % 10 = 7
So 15231-63-7 is a valid CAS Registry Number.
15231-63-7Relevant academic research and scientific papers
Sodium Borohydride Reduction of Adducts of Primary Amines with Aldehydes and p-Thiocresol. The Alkylation of Heterocyclic and Aromatic Amino-compounds
Kemal, Oeznur,Reese, Colin B.
, p. 1569 - 1573 (2007/10/02)
p-Nitroaniline, 2-aminopyridine (1a), 4-aminopyridine (2a), 2-amino-4-methylpyrimidine (8a), 2-aminothiazole (10a), and 2-aminobenzimidazole (12a) react with aqueous formaldehyde and p-thiocresol in ethanol or methanol solution to give N-(p-tolylthiomethyl) derivatives , usually in high yields.When the latter compounds are heated, under reflux, with an excess of sodium borohydride in ethanol or 1,2-dimethoxyethane solution, the corresponding methylamino-compounds are obtained.By a similar two-step prosedure in which aqueous formaldehyde is replaced, as appropriate, by anhydrous acetaldehyde, propionaldehyde, or benzaldehyde, p-nitroaniline is converted into N-ethyl-p-nitroaniline, p-chloroaniline is converted into p-chloro-N-(n-propyl)aniline, (1a) is converted into the corresponding ethylamino- and benzylamino-compounds (1c) and (1d), respectively, and (10a) and (12a) are converted into their 2-N-(n-propyl) derivatives (10c) and (12c), respectively.
