(S)-N-FMOC-beta-phenyl-beta-alanine
(S)-N-FMOC-3-Amino-3-phenylpropanoic acid
CAS: 209252-15-3
Molecular Formula: C24H21NO4
(S)-N-FMOC-beta-phenyl-beta-alanine - Names and Identifiers
(S)-N-FMOC-beta-phenyl-beta-alanine - Physico-chemical Properties
| Molecular Formula | C24H21NO4 |
| Molar Mass | 387.43 |
| Density | 1.2379 (rough estimate) |
| Melting Point | 187.3 °C |
| Boling Point | 513.39°C (rough estimate) |
| Flash Point | 326.9°C |
| Vapor Presure | 4.43E-16mmHg at 25°C |
| Appearance | White to light yellow powder |
| Color | White |
| BRN | 7982023 |
| pKa | 4.27±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.5614 (estimate) |
(S)-N-FMOC-beta-phenyl-beta-alanine - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29242990 |
| Hazard Class | IRRITANT |
(S)-N-FMOC-beta-phenyl-beta-alanine - Introduction
(S)-N-FMOC-3-Amino-3-phenylpropanoic acid is an organic compound commonly used in solid-phase synthesis. It has the following properties:
1. Appearance: white crystalline powder;
2. Molecular formula: c₂ H, NO;
3. Molecular weight: 357.39g/mol.
The main use of (S)-N-FMOC-3-Amino-3-phenylpropanoic acid is as an amino acid protecting group for the synthesis of polypeptides or proteins. It can synthesize polypeptides rich in aspartic acid, glutamic acid or other amino acids by solid phase synthesis.
In the preparation method, (S)-N-FMOC-3-Amino-3-phenylpropanoic acid can be synthesized by Fmoc protection reaction. The specific steps include reacting s-3-amino-3-phenylpropionic acid with Fmoc-Cl to produce (S)-N-FMOC-3-Amino-3-phenylpropanoic acid.
When using (S)-N-FMOC-3-Amino-3-phenylpropanoic acid, you need to pay attention to the following security information:
1. Skin contact may cause allergic reactions, so you should pay attention to wear appropriate personal protective equipment, such as laboratory gloves;
2. Avoid inhaling dust or gas, and ensure good ventilation;
3. If you accidentally come into contact with eyes or skin, rinse immediately with plenty of water and seek medical help;
4. Storage should be sealed, in the dark, dry, cool place.
1. Appearance: white crystalline powder;
2. Molecular formula: c₂ H, NO;
3. Molecular weight: 357.39g/mol.
The main use of (S)-N-FMOC-3-Amino-3-phenylpropanoic acid is as an amino acid protecting group for the synthesis of polypeptides or proteins. It can synthesize polypeptides rich in aspartic acid, glutamic acid or other amino acids by solid phase synthesis.
In the preparation method, (S)-N-FMOC-3-Amino-3-phenylpropanoic acid can be synthesized by Fmoc protection reaction. The specific steps include reacting s-3-amino-3-phenylpropionic acid with Fmoc-Cl to produce (S)-N-FMOC-3-Amino-3-phenylpropanoic acid.
When using (S)-N-FMOC-3-Amino-3-phenylpropanoic acid, you need to pay attention to the following security information:
1. Skin contact may cause allergic reactions, so you should pay attention to wear appropriate personal protective equipment, such as laboratory gloves;
2. Avoid inhaling dust or gas, and ensure good ventilation;
3. If you accidentally come into contact with eyes or skin, rinse immediately with plenty of water and seek medical help;
4. Storage should be sealed, in the dark, dry, cool place.
Last Update：2024-04-10 22:29:15
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CAS: 209252-15-3
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merry@highfine.com
QQ: 4006286883
CAS: 209252-15-3
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Email: chenmengqi@highfine.com
wuhao@highfine.com
merry@highfine.com
QQ: 4006286883
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View History
(S)-N-FMOC-beta-phenyl-beta-alanine
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-thiazolidineethanol dihydrogen phosphate
2,3-DIAMINOFLUOROBENZENE
(4-hydroxyphenyl)-2-butanone beta-d-glucoside
N-(2,4-DICHLOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE
Spiro[acridine-9(10H),9'-[9H]fluorene], 2,7-dimethyl-
1H-Thieno[3,4-d]imidazole-4-pentanamide, N-[3-[2-[2-(3-aminopropoxy)ethoxy]ethoxy]propyl]hexahydro-2-oxo-, (3aS,4S,6aR)-
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-thiazolidineethanol dihydrogen phosphate
2,3-DIAMINOFLUOROBENZENE
(4-hydroxyphenyl)-2-butanone beta-d-glucoside
N-(2,4-DICHLOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE
Spiro[acridine-9(10H),9'-[9H]fluorene], 2,7-dimethyl-
1H-Thieno[3,4-d]imidazole-4-pentanamide, N-[3-[2-[2-(3-aminopropoxy)ethoxy]ethoxy]propyl]hexahydro-2-oxo-, (3aS,4S,6aR)-