2-Iodophenyl Isothiocyanate
≥97%
- Product Code: 198898
CAS:
98041-44-2
| Molecular Weight: | 261.08 g./mol | Molecular Formula: | C₇H₄INS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00041057 | |
| Melting Point: | 36-39 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used primarily in organic synthesis as a versatile building block for pharmaceuticals and agrochemicals. Its isothiocyanate group readily reacts with nucleophiles such as amines and thiols, enabling the formation of thiourea and thioether derivatives, which are common motifs in bioactive molecules. The iodine substituent allows further functionalization via cross-coupling reactions like Suzuki or Heck couplings, making it valuable in the development of complex aromatic compounds. It is also employed in the preparation of heterocyclic compounds and functionalized dyes. Due to its dual reactivity, it serves as a key intermediate in medicinal chemistry for constructing libraries of compounds in drug discovery programs.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | $216.44 |
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| 1g | 10-20 days | $59.81 |
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2-Iodophenyl Isothiocyanate
Used primarily in organic synthesis as a versatile building block for pharmaceuticals and agrochemicals. Its isothiocyanate group readily reacts with nucleophiles such as amines and thiols, enabling the formation of thiourea and thioether derivatives, which are common motifs in bioactive molecules. The iodine substituent allows further functionalization via cross-coupling reactions like Suzuki or Heck couplings, making it valuable in the development of complex aromatic compounds. It is also employed in the preparation of heterocyclic compounds and functionalized dyes. Due to its dual reactivity, it serves as a key intermediate in medicinal chemistry for constructing libraries of compounds in drug discovery programs.
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