(R)-N-(TERT-BUTOXYCARBONYL)-BETA-PHENYL-PHENYLALN-(tert-Butoxycarbonyl)-beta-phenyl-D-phenylalanine ANINE
N-(tert-Butoxycarbonyl)-3-phenyl-D-phenylalanine
CAS: 143060-31-5;117027-46-0
Molecular Formula: C20H23NO4
(R)-N-(TERT-BUTOXYCARBONYL)-BETA-PHENYL-PHENYLALN-(tert-Butoxycarbonyl)-beta-phenyl-D-phenylalanine ANINE - Names and Identifiers
(R)-N-(TERT-BUTOXYCARBONYL)-BETA-PHENYL-PHENYLALN-(tert-Butoxycarbonyl)-beta-phenyl-D-phenylalanine ANINE - Physico-chemical Properties
| Molecular Formula | C20H23NO4 |
| Molar Mass | 341.4 |
| Density | 1.167±0.06 g/cm3(Predicted) |
| Melting Point | 157°C (dec.)(lit.) |
| Boling Point | 502.7±50.0 °C(Predicted) |
| pKa | 3.68±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.56 |
| Physical and Chemical Properties | Storage Conditions: Store at 0 ℃ WGK Germany:3 |
(R)-N-(TERT-BUTOXYCARBONYL)-BETA-PHENYL-PHENYLALN-(tert-Butoxycarbonyl)-beta-phenyl-D-phenylalanine ANINE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
(R)-N-(TERT-BUTOXYCARBONYL)-BETA-PHENYL-PHENYLALN-(tert-Butoxycarbonyl)-beta-phenyl-D-phenylalanine ANINE - Introduction
Boc-D-3, 3-diphenylalanine is an organic compound whose structure contains a protecting group (Boc group) and a D-form amino acid residue (D-3, 3-diphenylalanine). The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline powder
-Molecular formula: C22H25NO4
-Molecular Weight: 367.44 grams/mol
-Melting point: 102-106°C
-Soluble: Soluble in some organic solvents such as dimethylformamide (DMF) and dichloromethane (DCM)
Use:
- Boc-D-3, 3-diphenylalanine is a commonly used amino acid protecting group, which is used in the chemical synthesis of synthetic peptides and proteins.
-It can be used as a precursor compound in drug development and used to synthesize biologically active peptide drugs.
Preparation Method:
- Boc-D-3, 3-diphenylalanine is usually obtained by reacting D-3, 3-diphenylalanine with Boc acid chloride. The reaction can be carried out in an organic solvent, such as DMF or DCM, with the addition of a base as a catalyst.
Safety Information:
- Boc-D-3, the safety information of 3-diphenylalanine is limited, so appropriate personal protective measures should be taken when handling, such as wearing chemical protective gloves and protective glasses.
-Avoid inhaling its powder or solution, and avoid contact with skin and eyes.
-During use and storage, it should be sealed and kept away from fire and oxidizing agents.
Please note that the above information is for reference only. Before using this compound or conducting any experiments, please carefully read and follow the relevant chemical safety procedures and technical instructions.
Nature:
-Appearance: White crystalline powder
-Molecular formula: C22H25NO4
-Molecular Weight: 367.44 grams/mol
-Melting point: 102-106°C
-Soluble: Soluble in some organic solvents such as dimethylformamide (DMF) and dichloromethane (DCM)
Use:
- Boc-D-3, 3-diphenylalanine is a commonly used amino acid protecting group, which is used in the chemical synthesis of synthetic peptides and proteins.
-It can be used as a precursor compound in drug development and used to synthesize biologically active peptide drugs.
Preparation Method:
- Boc-D-3, 3-diphenylalanine is usually obtained by reacting D-3, 3-diphenylalanine with Boc acid chloride. The reaction can be carried out in an organic solvent, such as DMF or DCM, with the addition of a base as a catalyst.
Safety Information:
- Boc-D-3, the safety information of 3-diphenylalanine is limited, so appropriate personal protective measures should be taken when handling, such as wearing chemical protective gloves and protective glasses.
-Avoid inhaling its powder or solution, and avoid contact with skin and eyes.
-During use and storage, it should be sealed and kept away from fire and oxidizing agents.
Please note that the above information is for reference only. Before using this compound or conducting any experiments, please carefully read and follow the relevant chemical safety procedures and technical instructions.
Last Update：2024-04-09 20:49:11
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