1-Bromo-3-chloro-4-iodo-2-methylbenzene
97%
- Product Code: 114752
CAS:
1799612-41-1
| Molecular Weight: | 331.38 g./mol | Molecular Formula: | C₇H₅BrClI |
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| Density: | Storage Condition: | Avoid light, dry, room temperature |
Product Description:
1-Bromo-3-chloro-4-iodo-2-methylbenzene is primarily used in organic synthesis as a versatile intermediate for the production of more complex chemical compounds. Its multiple halogen substituents make it a valuable building block in cross-coupling reactions, such as Suzuki, Sonogashira, and Buchwald-Hartwig reactions, which are essential for creating pharmaceuticals, agrochemicals, and advanced materials. The presence of bromine, chlorine, and iodine allows for selective functionalization, enabling chemists to introduce specific groups at desired positions on the benzene ring. This compound is also utilized in the development of liquid crystals and organic electronic materials due to its structural rigidity and ability to form stable intermediates. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals, where its unique substitution pattern contributes to the desired properties of the final product.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿3,051.00 |
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| 1.000 | 10-20 days | ฿7,317.00 |
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1-Bromo-3-chloro-4-iodo-2-methylbenzene
1-Bromo-3-chloro-4-iodo-2-methylbenzene is primarily used in organic synthesis as a versatile intermediate for the production of more complex chemical compounds. Its multiple halogen substituents make it a valuable building block in cross-coupling reactions, such as Suzuki, Sonogashira, and Buchwald-Hartwig reactions, which are essential for creating pharmaceuticals, agrochemicals, and advanced materials. The presence of bromine, chlorine, and iodine allows for selective functionalization, enabling chemists to introduce specific groups at desired positions on the benzene ring. This compound is also utilized in the development of liquid crystals and organic electronic materials due to its structural rigidity and ability to form stable intermediates. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals, where its unique substitution pattern contributes to the desired properties of the final product.
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