112525-72-1
N-TERT-BUTOXYCARBONYL-DL-TRYPTOPHAN
CAS: 112525-72-1
Molecular Formula: C16H20N2O4
112525-72-1 - Names and Identifiers
112525-72-1 - Physico-chemical Properties
| Molecular Formula | C16H20N2O4 |
| Molar Mass | 304.34 |
| Density | 1.262±0.06 g/cm3(Predicted) |
| Melting Point | 131 °C(dec.) |
| Boling Point | 535.7±45.0 °C(Predicted) |
| pKa | 4.00±0.10(Predicted) |
| Storage Condition | 2-8°C |
112525-72-1 - Introduction
Boc-DL-Tryptophan is a chemical substance whose properties are as follows:
Nature:
1. Appearance: white or white solid;
2. molecular formula: C18H23NO5;
3. Molecular weight: 337.38g/mol;
4. Melting point: 78-81°C;
5. Solubility: Good solubility in common organic solvents.
Use:
Boc-DL-tryptophan is commonly used in the field of organic synthesis as an intermediate for amine protecting groups. It can be used in the synthesis of peptides, drugs and other organic compounds.
Preparation Method:
The preparation of Boc-DL-tryptophan usually requires the following steps:
1. starting with tryptophan;
2. Reaction with Boc-iminocarbamate to produce Boc-tryptophan;
3. by degradation or other methods, the protecting group is removed to obtain the Boc-DL-tryptophan product.
Safety Information:
Under the correct experimental operation, the use of Boc-DL-tryptophan is relatively safe. However, it is still a chemical substance and needs to be used in accordance with relevant safety procedures. When in contact, avoid direct inhalation of gas, contact with skin and eyes. Wear appropriate personal protective equipment such as lab gloves and goggles during use.
Nature:
1. Appearance: white or white solid;
2. molecular formula: C18H23NO5;
3. Molecular weight: 337.38g/mol;
4. Melting point: 78-81°C;
5. Solubility: Good solubility in common organic solvents.
Use:
Boc-DL-tryptophan is commonly used in the field of organic synthesis as an intermediate for amine protecting groups. It can be used in the synthesis of peptides, drugs and other organic compounds.
Preparation Method:
The preparation of Boc-DL-tryptophan usually requires the following steps:
1. starting with tryptophan;
2. Reaction with Boc-iminocarbamate to produce Boc-tryptophan;
3. by degradation or other methods, the protecting group is removed to obtain the Boc-DL-tryptophan product.
Safety Information:
Under the correct experimental operation, the use of Boc-DL-tryptophan is relatively safe. However, it is still a chemical substance and needs to be used in accordance with relevant safety procedures. When in contact, avoid direct inhalation of gas, contact with skin and eyes. Wear appropriate personal protective equipment such as lab gloves and goggles during use.
Last Update：2024-04-09 20:45:29
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View History
112525-72-1
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124387-19-5
propyleneglycolbeta-monoethylether
2-Chloro-6-fluorotol
萨利麝香 标准品
a-苯基苯甲醇
3-乙氧基-1-醇
2-吡啶-2-基乙醇
Andarine Impurity 25 (N-Nitroso Andarine Impurity)
Ammonium Stearate, Paste
124387-19-5
propyleneglycolbeta-monoethylether
2-Chloro-6-fluorotol
萨利麝香 标准品
a-苯基苯甲醇
3-乙氧基-1-醇
2-吡啶-2-基乙醇
Andarine Impurity 25 (N-Nitroso Andarine Impurity)