780752-32-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(bromomethyl)-4-methoxy-3,5-dimethylpyridine is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(bromomethyl)-4-methoxy-3,5-dimethylpyridine serves as a key intermediate in the synthesis of various agrochemicals. Its versatility in chemical reactions enables the production of effective pesticides, herbicides, and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used in Fine Chemicals Industry:
2-(bromomethyl)-4-methoxy-3,5-dimethylpyridine is also utilized in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, dyes, and specialty chemicals. Its presence in these compounds contributes to the development of high-quality products with specific properties.
It is crucial to handle 2-(bromomethyl)-4-methoxy-3,5-dimethylpyridine with care due to its reactive and potentially hazardous nature. Proper safety measures should be taken during its synthesis, storage, and use to ensure the safety of personnel and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 780752-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,0,7,5 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 780752-32:
(8*7)+(7*8)+(6*0)+(5*7)+(4*5)+(3*2)+(2*3)+(1*2)=181
181 % 10 = 1
So 780752-32-1 is a valid CAS Registry Number.
780752-32-1Relevant academic research and scientific papers
Joseph, Kara M.,Larraza-Sanchez, Isabel
, p. 13 - 16 (2011)
A series of benzyl bromides were efficiently prepared from the corresponding alcohols with Br3CCOCBr3/PPh3 at low temperatures and under neutral conditions. The present protocol was applied to the heterocyclic analogues and to the successful synthesis of the precursor of the antiulcer drug omeprazole, thus furnishing an alternate, mild method for the preparation of these drug intermediates. A significant steric factor was observed throughout both series supporting a SN2 mechanism.
