2-(2-bromo-3-nitrophenyl)acetonitrile
95%
- Product Code: 80702
CAS:
173026-24-9
| Molecular Weight: | 241.04 g./mol | Molecular Formula: | C₈H₅BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18392321 | |
| Melting Point: | Boiling Point: | 348.5±27.0 °C(Predicted) | |
| Density: | 1.677±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and nitro group, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic or heteroaromatic moieties into target compounds. Additionally, its nitrile group can be further functionalized into carboxylic acids, amides, or amines, expanding its utility in drug discovery and development. The compound is also explored in the synthesis of dyes and pigments due to its ability to modify electronic properties in organic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,020.00 |
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| 0.250 | 10-20 days | ฿11,700.00 |
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| 1.000 | 10-20 days | ฿23,400.00 |
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2-(2-bromo-3-nitrophenyl)acetonitrile
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and nitro group, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic or heteroaromatic moieties into target compounds. Additionally, its nitrile group can be further functionalized into carboxylic acids, amides, or amines, expanding its utility in drug discovery and development. The compound is also explored in the synthesis of dyes and pigments due to its ability to modify electronic properties in organic materials.
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