1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene
95%
- Product Code: 85799
CAS:
1359986-20-1
| Molecular Weight: | 308.01 g./mol | Molecular Formula: | C₁₀H₁₂Br₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22370201 | |
| Melting Point: | Boiling Point: | 320.7±37.0 °C at 760 mmHg | |
| Density: | 1.582±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis as a building block for the preparation of more complex molecules. Its structure, featuring bromine atoms and a methoxy group, makes it a valuable intermediate in the development of agrochemicals, particularly in the synthesis of herbicides and pesticides. The bromine atoms provide reactive sites for further functionalization, enabling the creation of compounds with specific biological activities. Additionally, it is employed in research settings for the study of aromatic substitution reactions, where its unique substitution pattern allows for the exploration of regioselectivity and reaction mechanisms. Its application extends to materials science, where it can be used in the synthesis of specialized polymers or organic electronic materials due to its aromatic core and functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft15,320.78 |
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| 5.000 | 10-20 days | Ft48,968.32 |
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| 10.000 | 10-20 days | Ft83,197.66 |
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1,2-Dibromo-4-methoxy-3,5,6-trimethylbenzene
This chemical is primarily utilized in the field of organic synthesis as a building block for the preparation of more complex molecules. Its structure, featuring bromine atoms and a methoxy group, makes it a valuable intermediate in the development of agrochemicals, particularly in the synthesis of herbicides and pesticides. The bromine atoms provide reactive sites for further functionalization, enabling the creation of compounds with specific biological activities. Additionally, it is employed in research settings for the study of aromatic substitution reactions, where its unique substitution pattern allows for the exploration of regioselectivity and reaction mechanisms. Its application extends to materials science, where it can be used in the synthesis of specialized polymers or organic electronic materials due to its aromatic core and functional groups.
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