The product, Factory Supply 2-amino-4,6-dimethylpyrimidine with CAS number 767 - 15 - 7, is offered at a low price. It belongs to the class of pyrimidine derivatives. Here are some of its basic parameters:
2 - amino - 4,6 - dimethylpyrimidine has a wide range of applications in different fields:
It serves as an important intermediate in the synthesis of various pharmaceutical compounds. It can be used to develop drugs with antibacterial, antiviral, and anti - inflammatory properties. For example, it can be used in the synthesis of some new - generation antibiotics that target specific bacterial strains.
In agriculture, it can be utilized in the production of pesticides and herbicides. Its unique chemical structure allows it to interact with certain enzymes in pests or weeds, disrupting their normal physiological functions and thereby achieving the purpose of pest control and weed suppression.
It is a valuable building block in organic synthesis. Chemists can use it to construct more complex organic molecules through various chemical reactions, such as coupling reactions and substitution reactions.
When using Factory Supply 2 - amino - 4,6 - dimethylpyrimidine, the following steps and precautions should be followed:
Always wear appropriate personal protective equipment (PPE), including gloves, safety glasses, and a lab coat. Avoid direct contact with the skin, eyes, and clothing. In case of contact, immediately rinse with plenty of water for at least 15 minutes and seek medical advice.
Store the product in a cool, dry, and well - ventilated place, away from sources of heat, ignition, and incompatible substances. Keep the container tightly closed when not in use.
When using it in chemical reactions, carefully calculate the appropriate dosage according to the reaction equation and experimental requirements. Control the reaction conditions such as temperature, pressure, and reaction time to ensure the smooth progress of the reaction.
A pharmaceutical company was developing a new antibacterial drug. They used 2 - amino - 4,6 - dimethylpyrimidine as an intermediate. First, they reacted it with a specific acyl chloride compound under reflux conditions in an organic solvent (such as dichloromethane) with a suitable base (such as triethylamine) as a catalyst. After a series of purification steps including extraction, distillation, and recrystallization, they obtained a key intermediate for the new drug. In subsequent in - vitro antibacterial tests, the new drug showed strong inhibitory effects on several common pathogenic bacteria, demonstrating the crucial role of 2 - amino - 4,6 - dimethylpyrimidine in the synthesis process.
An agricultural chemical research team was working on a new type of herbicide. They incorporated 2 - amino - 4,6 - dimethylpyrimidine into the molecular structure of the herbicide. Through field trials, they found that the new herbicide had excellent weed - killing effects on a variety of broad - leaf weeds. The unique pyrimidine structure of the product could
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