1-(4-Bromo-2-hydroxyphenyl)-2-(2,5-dibromophenyl)ethanone
97%
- Product Code: 39420
CAS:
1403991-85-4
| Molecular Weight: | 448.93 g./mol | Molecular Formula: | C₁₄H₉Br₃O₂ |
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| EC Number: | MDL Number: | MFCD29054043 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex compounds. It is particularly valuable in the development of pharmaceuticals and agrochemicals due to its brominated aromatic structure, which can facilitate further functionalization. The compound is also employed in research settings for studying reaction mechanisms involving halogenated phenols and ketones. Its unique structure makes it a potential candidate for the synthesis of materials with specific electronic or photophysical properties, such as organic semiconductors or fluorescent dyes. Additionally, it may be explored in the creation of bioactive molecules for therapeutic applications, given the presence of bromine atoms that can enhance binding affinity to biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,808.00 |
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1-(4-Bromo-2-hydroxyphenyl)-2-(2,5-dibromophenyl)ethanone
This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex compounds. It is particularly valuable in the development of pharmaceuticals and agrochemicals due to its brominated aromatic structure, which can facilitate further functionalization. The compound is also employed in research settings for studying reaction mechanisms involving halogenated phenols and ketones. Its unique structure makes it a potential candidate for the synthesis of materials with specific electronic or photophysical properties, such as organic semiconductors or fluorescent dyes. Additionally, it may be explored in the creation of bioactive molecules for therapeutic applications, given the presence of bromine atoms that can enhance binding affinity to biological targets.
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