35677-88-4
N-Carbobenzoxy-L-homoserine
CAS: 35677-88-4
Molecular Formula: C12H15NO5
35677-88-4 - Names and Identifiers
| Name | N-Carbobenzoxy-L-homoserine |
| Synonyms | Cbz-hse-OH Cbz-hse-OH Cbz-Homoserine Cbz-L-Homoserine Cbz-L-homoserine N-Carbobenzoxy-L-homoserine N-(Benzyloxycarbonyl)-L-homoserine Cbz-HoMoser Cbz-HoMoserine Cbz-Hse L-HoMoserine, N-[(phenylMethoxy)carbonyl]- 2-CarboxyaMino-4-hydroxybutyric acid, N-benzyl Ester |
| CAS | 35677-88-4 |
| InChI | InChI=1/C12H15NO5/c14-7-6-10(11(15)16)13-12(17)18-8-9-4-2-1-3-5-9/h1-5,10,14H,6-8H2,(H,13,17)(H,15,16)/t10-/m0/s1 |
35677-88-4 - Physico-chemical Properties
| Molecular Formula | C12H15NO5 |
| Molar Mass | 253.25 |
| Density | 1.311 |
| Melting Point | 100-101 °C |
| Boling Point | 519.9±50.0 °C(Predicted) |
| Flash Point | 268.2°C |
| Vapor Presure | 1.23E-11mmHg at 25°C |
| pKa | 3.85±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.563 |
35677-88-4 - Introduction
N-Carbobenzoxy-L-homoserine(N-Carbobenzoxy-L-homoserine) is an organic compound whose structure includes a benzoyl group and a homoserine group. Its chemical formula is C16H17NO5.
N-Carbobenzoxy-L-homoserine can be used as a derivative of amino acids, with the characteristics of benzyl ester group and homoserine. It is commonly used in organic synthesis as a protective group, which can protect the hydroxyl or amine group of homoserine to prevent damage in other reactions. In addition, it can also be used for the synthesis of peptides and proteins.
The method for preparing N-Carbobenzoxy-L-homoserine is usually to react homoserine with benzoyl chloride to generate the corresponding amide compound, and then to carry out hydroxyl protection reaction, finally obtaining the target product.
N-Carbobenzoxy-L-homoserine can be used as a derivative of amino acids, with the characteristics of benzyl ester group and homoserine. It is commonly used in organic synthesis as a protective group, which can protect the hydroxyl or amine group of homoserine to prevent damage in other reactions. In addition, it can also be used for the synthesis of peptides and proteins.
The method for preparing N-Carbobenzoxy-L-homoserine is usually to react homoserine with benzoyl chloride to generate the corresponding amide compound, and then to carry out hydroxyl protection reaction, finally obtaining the target product.
Last Update：2024-04-10 22:29:15
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