N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(3,4-DICHLOROPHENYL)BUTANOIC ACID
Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid
CAS: 270063-51-9
Molecular Formula: C15H19Cl2NO4
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(3,4-DICHLOROPHENYL)BUTANOIC ACID - Names and Identifiers
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(3,4-DICHLOROPHENYL)BUTANOIC ACID - Physico-chemical Properties
| Molecular Formula | C15H19Cl2NO4 |
| Molar Mass | 348.22 |
| Density | 1.294 |
| Boling Point | 494.8±45.0 °C(Predicted) |
| pKa | 4.36±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(3,4-DICHLOROPHENYL)BUTANOIC ACID - Risk and Safety
| Hazard Class | IRRITANT |
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(3,4-DICHLOROPHENYL)BUTANOIC ACID - Introduction
Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric is an organic compound with the following properties:
1. Appearance: White crystalline solid.
2. molecular formula: C19H22Cl2N2O4.
3. molecular weight: 410.29.
4. Solubility: Dissolved in common organic solvents.
5. Thermal stability: It has certain thermal stability and can be reacted under appropriate conditions.
The compound is commonly used in the epi-directional reaction in organic synthesis and is used as a chiral building block. It has the following main uses:
1. synthetic intermediate: Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid can be used as an intermediate for the synthesis of other organic compounds, such as drugs, pesticides and dyes.
2. Chiral synthesis: It can be used as a chiral inducer and chiral tool molecule to participate in chiral synthesis reactions and synthesize compounds with specific three-dimensional structures.
The method for preparing Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid generally includes the following steps:
1. an appropriate amount of 3,4-dichlorobenzoic acid and S-butoxycarbene reaction, S-3-amino -4-(3,4-dichlorophenyl) butyric acid.
2. Deprotection of S-3-amino -4-(3,4-dichlorophenyl) butyric acid to give Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid.
Regarding safety information, although there is no specific safety risk report, the following should be noted when handling this compound:
1. Avoid prolonged inhalation or contact with skin and use personal protective equipment (such as gloves and goggles).
2. Operate in a well-ventilated area and avoid inhaling its powder or vapor.
3. Comply with safe operation and correct waste disposal methods.
4. Avoid reaction with oxidants or other chemicals.
In view of the possible changes in safety and experimental conditions, please carefully read the safety data sheet (SDS) and laboratory guidelines for the compound before the experiment to ensure safe operation.
1. Appearance: White crystalline solid.
2. molecular formula: C19H22Cl2N2O4.
3. molecular weight: 410.29.
4. Solubility: Dissolved in common organic solvents.
5. Thermal stability: It has certain thermal stability and can be reacted under appropriate conditions.
The compound is commonly used in the epi-directional reaction in organic synthesis and is used as a chiral building block. It has the following main uses:
1. synthetic intermediate: Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid can be used as an intermediate for the synthesis of other organic compounds, such as drugs, pesticides and dyes.
2. Chiral synthesis: It can be used as a chiral inducer and chiral tool molecule to participate in chiral synthesis reactions and synthesize compounds with specific three-dimensional structures.
The method for preparing Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid generally includes the following steps:
1. an appropriate amount of 3,4-dichlorobenzoic acid and S-butoxycarbene reaction, S-3-amino -4-(3,4-dichlorophenyl) butyric acid.
2. Deprotection of S-3-amino -4-(3,4-dichlorophenyl) butyric acid to give Boc-(S)-3-Amino-4-3,4-dichloro-phenyl)-butyric acid.
Regarding safety information, although there is no specific safety risk report, the following should be noted when handling this compound:
1. Avoid prolonged inhalation or contact with skin and use personal protective equipment (such as gloves and goggles).
2. Operate in a well-ventilated area and avoid inhaling its powder or vapor.
3. Comply with safe operation and correct waste disposal methods.
4. Avoid reaction with oxidants or other chemicals.
In view of the possible changes in safety and experimental conditions, please carefully read the safety data sheet (SDS) and laboratory guidelines for the compound before the experiment to ensure safe operation.
Last Update：2024-04-09 20:02:46
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CAS: 270063-51-9
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CAS: 270063-51-9
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QQ: 3008007409
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