92028-39-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(benzyloxy)-5-methylpyridine is utilized as an intermediate in the synthesis of various pharmaceutical compounds. Its specific structural features allow it to serve as a key component in the development of new drugs, potentially contributing to the creation of medications with novel therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(benzyloxy)-5-methylpyridine is employed as a precursor in the production of certain agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in pest control, crop protection, and other agricultural applications, thereby enhancing crop yields and quality.
Used in Organic Synthesis:
2-(benzyloxy)-5-methylpyridine is used as a versatile building block in organic synthesis for the creation of a wide range of organic compounds. Its presence in various chemical reactions can lead to the formation of complex molecules with diverse applications in different fields, showcasing its utility in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 92028-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,2 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92028-39:
(7*9)+(6*2)+(5*0)+(4*2)+(3*8)+(2*3)+(1*9)=122
122 % 10 = 2
So 92028-39-2 is a valid CAS Registry Number.
92028-39-2Relevant academic research and scientific papers
Preparation of N-alkyl 2-pyridones via a lithium iodide promoted oto N-alkyl migration: Scope and mechanism
Tasker, Sarah Z.,Bosscher, Michael A.,Shandro, Christina A.,Ryu, Keun Ah,Snapper, Gregory S.,Utter, Jarrad M.,Anderson, Carolyn E.,Lanni, Erica L.,Ellsworth, Bruce A.
, p. 8220 - 8230,11 (2020/10/15)
An efficient and inexpensive LiI-promoted O- to N-alkyl migration of 2-benzyloxy-, 2-allyloxy-, and 2-propargyloxypyridines and heterocycles is reported. The reaction produces the corresponding N-alkyl 2-pyridones and analogues under green, solvent-free conditions in good to excellent yields (30 examples, 20-97% yield). This method has been shown to be intermolecular and requires heat and lithium cation to occur.
Synthesis of substituted N-benzyl pyridones via an O- To N-alkyl migration
Lanni, Erica L.,Bosscher, Michael A.,Ooms, Bartel D.,Shandro, Christina A.,Ellsworth, Bruce A.,Anderson, Carolyn E.
, p. 6425 - 6428 (2008/12/21)
(Chemical Equation Presented) A new LiI-promoted O- to N-alkyl migration has been developed for the conversion of O-alkylated 2-hydroxy pyridines, quinolines, and pyrimidines to the corresponding N-alkylated heterocycles in good to excellent yields (57-99%). This method serves as an efficient means for the preparation of N-benzyl pyridones, quinolones, and pyrimidones.
