(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopyrrolidin-3-yl)propanoate
Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl]propanoate
CAS: 328086-60-8
Molecular Formula: C13H22N2O5
(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopyrrolidin-3-yl)propanoate - Names and Identifiers
(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopyrrolidin-3-yl)propanoate - Physico-chemical Properties
| Molecular Formula | C13H22N2O5 |
| Molar Mass | 286.32 |
| Density | 1.142±0.06 g/cm3(Predicted) |
| Boling Point | 471.5±20.0 °C(Predicted) |
| Storage Condition | 2-8℃ |
| Physical and Chemical Properties | Acidity coefficient (pKa) 10.97±0.46(Predicted) |
| Use | (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl] methyl propionate is a carboxylate organic substance, which can be used as a pharmaceutical intermediate. |
(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopyrrolidin-3-yl)propanoate - Introduction
Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-yrrolidinyl] propanoate is an organic compound with the following properties:
1. Appearance: colorless to light yellow crystal or powder;
2. molecular formula: C14H23NO5;
3. Molecular weight: 281.34g/mol;
4. Solubility: Soluble in some organic solvents, such as ethanol, dimethylformamide (DMF) and dichloromethane;
5. Melting point: about 48-50°C.
It is mainly used as an intermediate in organic synthesis reactions, and the specific applications are as follows:
1. Drug development: can be used as an intermediate for the synthesis of peptide drugs, commonly used in the synthesis of peptides, proteins or drug precursors;
2. Biochemistry: It can be used to synthesize and modify specific amino acid sequences in the fields of proteomics, enzymology and medicinal chemistry;
3. Chemical synthesis: It can be used to prepare chiral compounds to enhance the research and application of chiral molecules.
The method for preparing Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl]propanoate is as follows:
1. (S)-2-oxo-3-pyrrolidinyl ethanol and N,N'-dimethylformamide dioxane are used as reactants and reacted at an appropriate temperature to produce (S)-2-oxo-3-pyrrolidinyl dimethylamide;
2. Reaction of (S)-2-oxo-3-pyrrolidinyldicarboxamide with Boc-methyl carbamate to give Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl]propanoate.
Regarding safety information, this compound is a reagent used in organic synthesis, and the following should be noted:
1. avoid contact with skin and eyes, pay close attention to personal protective measures;
2. when in use, it should be operated in a well-ventilated place to avoid inhaling the dust or gas of the substance;
3. storage should be stored in a dry, ventilated place, avoid contact with oxygen, moisture and combustibles;
4. For the sake of safety, it is recommended to operate in a professional chemical laboratory and strictly abide by the corresponding safety operation procedures.
It should be noted that the above information is for reference only, and relevant chemical literature and safety data sheets should be referred to for specific use.
1. Appearance: colorless to light yellow crystal or powder;
2. molecular formula: C14H23NO5;
3. Molecular weight: 281.34g/mol;
4. Solubility: Soluble in some organic solvents, such as ethanol, dimethylformamide (DMF) and dichloromethane;
5. Melting point: about 48-50°C.
It is mainly used as an intermediate in organic synthesis reactions, and the specific applications are as follows:
1. Drug development: can be used as an intermediate for the synthesis of peptide drugs, commonly used in the synthesis of peptides, proteins or drug precursors;
2. Biochemistry: It can be used to synthesize and modify specific amino acid sequences in the fields of proteomics, enzymology and medicinal chemistry;
3. Chemical synthesis: It can be used to prepare chiral compounds to enhance the research and application of chiral molecules.
The method for preparing Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl]propanoate is as follows:
1. (S)-2-oxo-3-pyrrolidinyl ethanol and N,N'-dimethylformamide dioxane are used as reactants and reacted at an appropriate temperature to produce (S)-2-oxo-3-pyrrolidinyl dimethylamide;
2. Reaction of (S)-2-oxo-3-pyrrolidinyldicarboxamide with Boc-methyl carbamate to give Methyl (S)-2-(Boc-amino)-3-[(S)-2-oxo-3-pyrrolidinyl]propanoate.
Regarding safety information, this compound is a reagent used in organic synthesis, and the following should be noted:
1. avoid contact with skin and eyes, pay close attention to personal protective measures;
2. when in use, it should be operated in a well-ventilated place to avoid inhaling the dust or gas of the substance;
3. storage should be stored in a dry, ventilated place, avoid contact with oxygen, moisture and combustibles;
4. For the sake of safety, it is recommended to operate in a professional chemical laboratory and strictly abide by the corresponding safety operation procedures.
It should be noted that the above information is for reference only, and relevant chemical literature and safety data sheets should be referred to for specific use.
Last Update：2024-04-09 20:02:46
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