(2-Bromophenyl)(4-chlorophenyl)methanone
95%
- Product Code: 64717
CAS:
99585-64-5
| Molecular Weight: | 295.56 g./mol | Molecular Formula: | C₁₃H₈BrClO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08063806 | |
| Melting Point: | Boiling Point: | 381.5±22.0 °C(Predicted) | |
| Density: | 1.510±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a valuable building block in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Ullmann reactions, to create biaryl compounds, which are essential in drug discovery and material science. Additionally, it serves as a precursor in the synthesis of specialty chemicals, including dyes, pigments, and polymers, where its halogenated aromatic rings contribute to desired properties like stability and reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,861.00 |
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| 0.250 | 10-20 days | ฿7,020.00 |
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| 1.000 | 10-20 days | ฿14,040.00 |
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(2-Bromophenyl)(4-chlorophenyl)methanone
This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a valuable building block in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Ullmann reactions, to create biaryl compounds, which are essential in drug discovery and material science. Additionally, it serves as a precursor in the synthesis of specialty chemicals, including dyes, pigments, and polymers, where its halogenated aromatic rings contribute to desired properties like stability and reactivity.
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