273221-75-3
boc-l-3-iodophenylalanine
CAS: 273221-75-3
Molecular Formula: C14H18INO4
273221-75-3 - Names and Identifiers
273221-75-3 - Physico-chemical Properties
| Molecular Formula | C14H18INO4 |
| Molar Mass | 391.2 |
| Density | 1.560±0.06 g/cm3(Predicted) |
| Boling Point | 491.6±45.0 °C(Predicted) |
| pKa | 3.82±0.10(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
273221-75-3 - Risk and Safety
| Hazard Class | IRRITANT |
273221-75-3 - Introduction
boc-l-3-iodophenylalanine is an organic compound with the chemical formula C17H21INO4. It is an amino acid derivative with a protective group (Boc Group) and an iodine atom substituted phenylalanine.
boc-l-3-iodophenylalanine are commonly used in biochemical research, especially in the fields of peptide synthesis and protein engineering. It can be used as a starting point for the synthesis of new peptide drugs, and can also be used to label proteins or peptide segments to facilitate their location, tracking or research.
The preparation method of boc-l-3-iodophenylalanine can be obtained by reacting phenylalanine with stannous iodide. First, phenylalanine is reacted with stannous iodide in the presence of ethanol to produce boc-l-3-iodophenylalanine. Then, the resultant was purified and crystallized.
Need to pay attention to safety when using boc-l-3-iodophenylalanine. It is a chemical that can be toxic and irritating. Contact with skin, eyes and respiratory tract should be avoided. Appropriate protective equipment such as lab gloves, goggles and protective masks should be worn during operation. In addition, the operation should be carried out under well-ventilated laboratory conditions to avoid inhalation of dust or vapors. In case of accidental contact or inhalation, wash the affected area immediately and seek medical help.
boc-l-3-iodophenylalanine are commonly used in biochemical research, especially in the fields of peptide synthesis and protein engineering. It can be used as a starting point for the synthesis of new peptide drugs, and can also be used to label proteins or peptide segments to facilitate their location, tracking or research.
The preparation method of boc-l-3-iodophenylalanine can be obtained by reacting phenylalanine with stannous iodide. First, phenylalanine is reacted with stannous iodide in the presence of ethanol to produce boc-l-3-iodophenylalanine. Then, the resultant was purified and crystallized.
Need to pay attention to safety when using boc-l-3-iodophenylalanine. It is a chemical that can be toxic and irritating. Contact with skin, eyes and respiratory tract should be avoided. Appropriate protective equipment such as lab gloves, goggles and protective masks should be worn during operation. In addition, the operation should be carried out under well-ventilated laboratory conditions to avoid inhalation of dust or vapors. In case of accidental contact or inhalation, wash the affected area immediately and seek medical help.
Last Update：2024-04-09 21:01:54
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