Tert-butyl (4-hydroxy-3-iodophenethyl)carbamate
97%
- Product Code: 238446
Alias:
tert-Butyl 4-hydroxy-3-iodophenethylcarbamate; N-tert-Butoxycarbonyl 3-Iodotyramine; [2-(4-Hydroxy-3-iodophenyl)ethyl]carbaMicAcid1,1-DiMethylethylEster; N-(tert-Butoxycarbonyl)[2-(4-hydroxy-3-iodophenyl)ethyl]aMine;tert-Butyl4Chemicalbook-hydroxy-3-iodop
CAS:
788824-50-0
Properties:
Soluble in chloroform (a little), ethyl acetate (a little), methanol (a little)
| Molecular Weight: | 363.19 g./mol | Molecular Formula: | C₁₃H₁₈INO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07779453 | |
| Melting Point: | 129-130 °C | Boiling Point: | 412.0±40.0 °C(Predicted) |
| Density: | 1.528±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. The iodine moiety allows for incorporation of radioactive isotopes such as iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). Its protected amine group facilitates selective reactions in multi-step organic syntheses, especially in the preparation of bioactive molecules targeting neurological and endocrine systems. Also employed in the production of specialty reagents for research in receptor binding and metabolic pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $333.13 |
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| 1.000 | 10-20 days | $1,451.58 |
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| 5.000 | 10-20 days | $5,805.38 |
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| 0.250 | 10-20 days | $696.97 |
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Tert-butyl (4-hydroxy-3-iodophenethyl)carbamate
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. The iodine moiety allows for incorporation of radioactive isotopes such as iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). Its protected amine group facilitates selective reactions in multi-step organic syntheses, especially in the preparation of bioactive molecules targeting neurological and endocrine systems. Also employed in the production of specialty reagents for research in receptor binding and metabolic pathways.
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