(S)-3-(tert-butoxycarbonylamino)-3-(4-hydr
Boc-S-3-Amino-3-(4-hydroxy-phenyl)-propionic acid
CAS:
Molecular Formula: C14H19NO5
(S)-3-(tert-butoxycarbonylamino)-3-(4-hydr - Names and Identifiers
(S)-3-(tert-butoxycarbonylamino)-3-(4-hydr - Physico-chemical Properties
| Molecular Formula | C14H19NO5 |
| Molar Mass | 281.3 |
| Density | 1.236±0.06 g/cm3(Predicted) |
| Boling Point | 476.7±40.0 °C(Predicted) |
| pKa | 4.41±0.10(Predicted) |
| Storage Condition | 2-8°C |
(S)-3-(tert-butoxycarbonylamino)-3-(4-hydr - Risk and Safety
| WGK Germany | 3 |
(S)-3-(tert-butoxycarbonylamino)-3-(4-hydr - Introduction
Boc-S-3-Amino-3-(4-hydroxy-phenyl)-propionic acid is an organic compound with the following properties:
1. Appearance: white crystalline powder.
2. molecular formula: C14H19NO5.
3. Molecular weight: 285.31g/mol.
4. Melting point: about 106-109°C.
5. solubility: can be dissolved in organic solvents (such as dimethyl sulfoxide, chloroform), insoluble in water.
The main uses of Boc-S-3-Amino-3-(4-hydroxy-phenyl)-propionic acid include:
1. biochemical research: can be used as a protective group for synthetic peptides or proteins.
2. Drug development: can be used to design and synthesize compounds with biological activity.
3. chemical synthesis: can be used as a starting material or intermediate in organic synthesis.
The production method of Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid is generally obtained by an organic synthesis method. The specific preparation method is as follows:
1. The 3-amino -3-(4-hydroxyphenyl) propionic acid reactant is reacted with tert-butyl oxycarbonylhydrazine (Boc-ONH2) in an appropriate solvent.
2. After reaction, the product Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid was obtained.
3. Finally, the pure product is obtained by appropriate separation and purification methods, such as crystallization or column chromatography.
When using Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid, the following safety information should be noted:
1. Wear appropriate protective equipment, such as laboratory gloves and goggles.
2. Avoid direct contact with skin, eyes and mucous membranes. In case of contact, rinse immediately with plenty of water and seek medical attention if necessary.
3. Avoid dust or aerosols during operation to avoid inhaling them.
4. During storage and handling, care should be taken to avoid contact with oxidants and combustibles to prevent fire or explosion.
1. Appearance: white crystalline powder.
2. molecular formula: C14H19NO5.
3. Molecular weight: 285.31g/mol.
4. Melting point: about 106-109°C.
5. solubility: can be dissolved in organic solvents (such as dimethyl sulfoxide, chloroform), insoluble in water.
The main uses of Boc-S-3-Amino-3-(4-hydroxy-phenyl)-propionic acid include:
1. biochemical research: can be used as a protective group for synthetic peptides or proteins.
2. Drug development: can be used to design and synthesize compounds with biological activity.
3. chemical synthesis: can be used as a starting material or intermediate in organic synthesis.
The production method of Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid is generally obtained by an organic synthesis method. The specific preparation method is as follows:
1. The 3-amino -3-(4-hydroxyphenyl) propionic acid reactant is reacted with tert-butyl oxycarbonylhydrazine (Boc-ONH2) in an appropriate solvent.
2. After reaction, the product Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid was obtained.
3. Finally, the pure product is obtained by appropriate separation and purification methods, such as crystallization or column chromatography.
When using Boc-S-3-amino -3-(4-hydroxyphenyl) propionic acid, the following safety information should be noted:
1. Wear appropriate protective equipment, such as laboratory gloves and goggles.
2. Avoid direct contact with skin, eyes and mucous membranes. In case of contact, rinse immediately with plenty of water and seek medical attention if necessary.
3. Avoid dust or aerosols during operation to avoid inhaling them.
4. During storage and handling, care should be taken to avoid contact with oxidants and combustibles to prevent fire or explosion.
Last Update：2024-04-09 21:21:28
