2-Bromo-5-iodo-4-nitrobenzotrifluoride
≥97%
- Product Code: 71747
CAS:
1187385-82-5
| Molecular Weight: | 395.8999596 g./mol | Molecular Formula: | C₇H₂BrF₃INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12913962 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring bromo, iodo, nitro, and trifluoromethyl groups, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of multiple reactive sites allows for selective functionalization, enabling the creation of diverse compounds. It is particularly useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, where the halogen atoms can be substituted to form carbon-carbon or carbon-heteroatom bonds. Additionally, the nitro group can be reduced to an amine, further expanding its utility in synthesizing biologically active compounds. Its trifluoromethyl group is often retained in the final product, as it can enhance stability, lipophilicity, and metabolic resistance, which are desirable properties in drug design.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow Powder |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,220.00 |
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| 1.000 | 10-20 days | ฿25,390.00 |
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2-Bromo-5-iodo-4-nitrobenzotrifluoride
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring bromo, iodo, nitro, and trifluoromethyl groups, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of multiple reactive sites allows for selective functionalization, enabling the creation of diverse compounds. It is particularly useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, where the halogen atoms can be substituted to form carbon-carbon or carbon-heteroatom bonds. Additionally, the nitro group can be reduced to an amine, further expanding its utility in synthesizing biologically active compounds. Its trifluoromethyl group is often retained in the final product, as it can enhance stability, lipophilicity, and metabolic resistance, which are desirable properties in drug design.
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