4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile
≥97%
- Product Code: 81139
CAS:
460746-47-8
Molecular Weight: | 321.11 g./mol | Molecular Formula: | C₁₃H₈INO |
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EC Number: | MDL Number: | MFCD06796628 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dark, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical structures. Its unique structure, featuring both hydroxyl and iodo groups, makes it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. The compound is particularly useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for creating carbon-carbon bonds in drug discovery and material science. Additionally, its biphenyl core and functional groups allow for further modifications, enabling the production of compounds with potential biological activity. It is also explored in the development of liquid crystals and organic electronic materials due to its rigid aromatic framework and ability to form stable molecular arrangements.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | €34.19 |
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1.000 | 10-20 days | €86.66 |
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5.000 | 10-20 days | €272.82 |
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4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile
This compound is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical structures. Its unique structure, featuring both hydroxyl and iodo groups, makes it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. The compound is particularly useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for creating carbon-carbon bonds in drug discovery and material science. Additionally, its biphenyl core and functional groups allow for further modifications, enabling the production of compounds with potential biological activity. It is also explored in the development of liquid crystals and organic electronic materials due to its rigid aromatic framework and ability to form stable molecular arrangements.
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