N-[(PHENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID 1-(PHENYLMETHYL) ESTER
Z-Asp-OBzl
CAS: 4779-31-1
Molecular Formula: C19H19NO6
N-[(PHENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID 1-(PHENYLMETHYL) ESTER - Names and Identifiers
| Name | Z-Asp-OBzl |
| Synonyms | Z-Asp-OBzl CBZ-ASP-OBZL CBZ-L-ASP-ALPHA-BENZYL ESTER Z-L-ASPARTIC ACID A-BENZYLESTER Z-L-aspartic acid α-benzyl ester CBZ-L-ASPARTIC ACID A-BENZYL ESTER N-Benzyloxycarbonyl-L-aspartic acid ALPHA-benzyl ester N-[(PHENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID 1-(PHENYLMETHYL) ESTER Cbz-Asp-OBZL-OH,(S)-4-(benzyloxy)-3-(benzyloxycarbonylamino)-4-oxobutanoic acid 4-(benzyloxy)-3-{[(benzyloxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name) (3S)-4-(benzyloxy)-3-{[(benzyloxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name) |
| CAS | 4779-31-1 |
| InChI | InChI=1/C19H19NO6/c21-17(22)11-16(18(23)25-12-14-7-3-1-4-8-14)20-19(24)26-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,20,24)(H,21,22)/t16-/m0/s1 |
N-[(PHENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID 1-(PHENYLMETHYL) ESTER - Physico-chemical Properties
| Molecular Formula | C19H19NO6 |
| Molar Mass | 357.36 |
| Density | 1.293±0.06 g/cm3(Predicted) |
| Melting Point | 83-85°C |
| Boling Point | 583.5±50.0 °C(Predicted) |
| Flash Point | 306.7°C |
| Solubility | Acetone, Chloroform, DMSO, Ether, Methanol |
| Vapor Presure | 1.85E-14mmHg at 25°C |
| Appearance | Solid |
| Color | Colourless to White |
| pKa | 4.09±0.19(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.581 |
N-[(PHENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID 1-(PHENYLMETHYL) ESTER - Introduction
Z-Asp-OBzl (Z-Asp-OBzl) is a chemical compound containing benzyl ester and aspartic acid groups in its chemical structure. The following is a description of some properties, uses, preparation and safety information about the compound:
Nature:
-Appearance: The compound is white or off-white crystal
-Molecular formula: C18H19NO6
-Molecular weight: 349.35g/mol
-Melting point: about 75-76 degrees Celsius
-Solubility: Soluble in ethanol, chloroform, dichloromethane and other organic solvents
Use:
-Drug research: Z-Asp-OBzl, as an aspartic acid derivative, is commonly used in drug research to synthesize antiviral, anti-tumor, anti-inflammatory and other compounds.
-Biochemical research: This compound is usually used as a synthetic intermediate in chemical synthesis, used to synthesize more complex compounds or study the catalytic reaction mechanism of enzymes.
Preparation Method:
The synthesis of Z-Asp-OBzl usually involves the methods and techniques of organic synthetic chemistry, which can generally be prepared by the following steps:
1. benzoic acid reacts with the reagent benzyl ammonium bromide to generate benzyl benzoic acid.
2. reacting benzyl benzoic acid with dimethyl sulfoxide to generate dimethyl sulfoxide of benzyl benzoate.
3. using the method of replacing the reagent, the reaction generates the final Z-Asp-OBzl product.
Safety Information:
- Z-Asp-OBzl toxicity information is limited, under normal circumstances, it will not bring greater harm to the human body in the case of reasonable use.
-However, any chemical should be stored and used under appropriate conditions. During the operation, the relevant laboratory safety procedures should be followed to avoid direct contact with the compound.
-During disposal, the relevant environmental and regulatory requirements should be met.
Please note that the above information is for reference only. If you need to apply and use the compound, it is recommended to operate under the guidance of professionals.
Nature:
-Appearance: The compound is white or off-white crystal
-Molecular formula: C18H19NO6
-Molecular weight: 349.35g/mol
-Melting point: about 75-76 degrees Celsius
-Solubility: Soluble in ethanol, chloroform, dichloromethane and other organic solvents
Use:
-Drug research: Z-Asp-OBzl, as an aspartic acid derivative, is commonly used in drug research to synthesize antiviral, anti-tumor, anti-inflammatory and other compounds.
-Biochemical research: This compound is usually used as a synthetic intermediate in chemical synthesis, used to synthesize more complex compounds or study the catalytic reaction mechanism of enzymes.
Preparation Method:
The synthesis of Z-Asp-OBzl usually involves the methods and techniques of organic synthetic chemistry, which can generally be prepared by the following steps:
1. benzoic acid reacts with the reagent benzyl ammonium bromide to generate benzyl benzoic acid.
2. reacting benzyl benzoic acid with dimethyl sulfoxide to generate dimethyl sulfoxide of benzyl benzoate.
3. using the method of replacing the reagent, the reaction generates the final Z-Asp-OBzl product.
Safety Information:
- Z-Asp-OBzl toxicity information is limited, under normal circumstances, it will not bring greater harm to the human body in the case of reasonable use.
-However, any chemical should be stored and used under appropriate conditions. During the operation, the relevant laboratory safety procedures should be followed to avoid direct contact with the compound.
-During disposal, the relevant environmental and regulatory requirements should be met.
Please note that the above information is for reference only. If you need to apply and use the compound, it is recommended to operate under the guidance of professionals.
Last Update：2024-04-09 20:45:29
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