N-ALPHA-CARBOBENZOXY-L-2-AMINOADIPIC ACID
Z-L-.alpha.-aminoadipic acid
CAS: 24325-14-2
Molecular Formula: C14H17NO6
N-ALPHA-CARBOBENZOXY-L-2-AMINOADIPIC ACID - Names and Identifiers
N-ALPHA-CARBOBENZOXY-L-2-AMINOADIPIC ACID - Physico-chemical Properties
| Molecular Formula | C14H17NO6 |
| Molar Mass | 295.29 |
| Density | 1.322±0.06 g/cm3(Predicted) |
| Melting Point | 163℃ |
| Boling Point | 551.9±50.0 °C(Predicted) |
| pKa | 3.91±0.21(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
N-ALPHA-CARBOBENZOXY-L-2-AMINOADIPIC ACID - Introduction
Z-L-.alpha.-aminoadipic acid is a compound with the formula Z-L-.alpha.-aminoadipic acid. It is a white crystalline solid with high chemical stability.
Z-L-.alpha.-aminoadipic acid is often used as a reagent for protecting amino acids. It can protect the amino function in the α-amino acid, and the protecting group can be removed by heating or acidic conditions when necessary. Therefore, it plays an important role in the synthesis of bioactive molecules, peptides, proteins and drugs.
Preparation Z-L-.alpha. The method of-aminoadipic acid is to react L-2-aminoadipic acid with N-tert-butoxycarbonyl affinity mixture (Z-Cl) to generate Z-L-.alpha.-aminoadipic acid. This process needs to be carried out under appropriate reaction conditions, usually under an inert atmosphere, and can be extracted by crystallization or other separation and purification methods after the reaction is completed.
For security information, Z-L-.alpha.-aminoadipic acid has no specific security risk under regular operation. However, as a compound, care should be taken to avoid inhalation, ingestion, or contact with the skin and eyes. During use, laboratory safety procedures should be followed and personal protective equipment such as laboratory gloves and eye protection should be used.
Z-L-.alpha.-aminoadipic acid is often used as a reagent for protecting amino acids. It can protect the amino function in the α-amino acid, and the protecting group can be removed by heating or acidic conditions when necessary. Therefore, it plays an important role in the synthesis of bioactive molecules, peptides, proteins and drugs.
Preparation Z-L-.alpha. The method of-aminoadipic acid is to react L-2-aminoadipic acid with N-tert-butoxycarbonyl affinity mixture (Z-Cl) to generate Z-L-.alpha.-aminoadipic acid. This process needs to be carried out under appropriate reaction conditions, usually under an inert atmosphere, and can be extracted by crystallization or other separation and purification methods after the reaction is completed.
For security information, Z-L-.alpha.-aminoadipic acid has no specific security risk under regular operation. However, as a compound, care should be taken to avoid inhalation, ingestion, or contact with the skin and eyes. During use, laboratory safety procedures should be followed and personal protective equipment such as laboratory gloves and eye protection should be used.
Last Update：2024-04-09 20:45:29
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CAS: 24325-14-2
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CAS: 24325-14-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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