4-Bromobenzonitrile
98%
- Product Code: 119408
Alias:
4-bromocyanobenzene; p-bromobenzonitrile; p-bromobenzonitrile; p-bromocyanobenzene; 4-bromobenzonitrile; 4-bromobenzonitrile;
CAS:
623-00-7
Molecular Weight: | 182.02 g./mol | Molecular Formula: | C₇H₄BrN |
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EC Number: | MDL Number: | MFCD00001811 | |
Melting Point: | 110-115 °C(lit.) | Boiling Point: | 235-237 °C(lit.) |
Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, 4-Bromobenzonitrile serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it valuable in constructing complex organic molecules. It is also employed in the development of liquid crystals and electronic materials due to its aromatic and nitrile functional groups, which contribute to stability and polarity. Additionally, it finds use in research for studying reaction mechanisms and developing new synthetic pathways.
Product Specification:
Test | Specification |
---|---|
Carbon | 45.4-45.8 |
Nitrogen | 7.5-7.9 |
Purity (%) | 97.5-100 |
Melting Point | 111-114 |
Appearance | WHITE TO LIGHT YELLOW POWDER OR CRYSTALS |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿290.00 |
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25.000 | 10-20 days | ฿660.00 |
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100.000 | 10-20 days | ฿2,280.00 |
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500.000 | 10-20 days | ฿10,870.00 |
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4-Bromobenzonitrile
Used primarily in organic synthesis, 4-Bromobenzonitrile serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it valuable in constructing complex organic molecules. It is also employed in the development of liquid crystals and electronic materials due to its aromatic and nitrile functional groups, which contribute to stability and polarity. Additionally, it finds use in research for studying reaction mechanisms and developing new synthetic pathways.
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