(2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate
N-epsilon-cbz-D-lysine
CAS: 34404-32-5
Molecular Formula: C14H20N2O4
(2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate - Names and Identifiers
| Name | N-epsilon-cbz-D-lysine |
| Synonyms | z-D-Lysine
H-D-Lys(Z)-OH H-D-LYS(Z)-OH N-e-CBZ-D-Lys N6-Cbz-D-lysine N-e-CBZ-D-Lysine N-EPSILON-Z-D-LYSINE N-epsilon-cbz-D-lysine N-EPSILON-CBZ-D-LYSINE N-EPSILON-CARBOBENZOXY-D-LYSINE N~6~-[(benzyloxy)carbonyl]lysine Nepsilon-carbobenzyloxy-D-lysine N-EPSILON-BENZYLOXYCARBONYL-D-LYSINE N6-[(PHENYLMETHOXY)CARBONYL]-R-LYSINE 2-amino-6-(benzyloxycarbonylamino)hexanoic acid (2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate |
| CAS | 34404-32-5 |
| EINECS | 214-585-7 |
| InChI | InChI=1/C14H20N2O4/c15-12(13(17)18)8-4-5-9-16-14(19)20-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,15H2,(H,16,19)(H,17,18)/t12-/m1/s1 |
(2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate - Physico-chemical Properties
| Molecular Formula | C14H20N2O4 |
| Molar Mass | 280.32 |
| Density | 1.206±0.06 g/cm3(Predicted) |
| Melting Point | 229℃ |
| Boling Point | 499.6±45.0 °C(Predicted) |
| Flash Point | 255.9°C |
| Vapor Presure | 8.43E-11mmHg at 25°C |
| Appearance | Powder |
| Color | White |
| pKa | 2.53±0.24(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.55 |
(2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate - Risk and Safety
| WGK Germany | 3 |
(2R)-2-ammonio-6-{[(benzyloxy)carbonyl]amino}hexanoate - Introduction
N-epsilon-cbz-D-lysine is a chemical compound whose chemical name is N-epsilon-cbz-D-lysine. It is a derivative of lysine and has certain properties and uses.
N-epsilon-cbz-D-lysine are commonly used in biochemistry and medicinal chemistry research as important intermediates for the synthesis and modification of peptides or proteins. It can be used to synthesize compounds such as modified peptides, protein drugs or fluorescent probes.
The method for preparing N-epsilon-cbz-D-lysine is usually obtained by reacting lysine with a carboxylic acid protecting group (Cbz). The reaction can be carried out using common organic synthesis methods under appropriate reaction conditions.
N-epsilon-cbz-D-lysine safety information is limited, so appropriate laboratory procedures and personal protective measures should be followed when using or handling this compound. It may cause irritation or other adverse reactions to the human body, so it is recommended to use it under suitable experimental conditions and follow relevant safety guidelines.
Please note that the information provided above is for informational purposes only. Reference should also be made to the relevant literature and safety data sheets for specific applications and operations. When using this compound, it is recommended that it be carried out in a suitable laboratory environment and to ensure that laboratory safety procedures are followed.
N-epsilon-cbz-D-lysine are commonly used in biochemistry and medicinal chemistry research as important intermediates for the synthesis and modification of peptides or proteins. It can be used to synthesize compounds such as modified peptides, protein drugs or fluorescent probes.
The method for preparing N-epsilon-cbz-D-lysine is usually obtained by reacting lysine with a carboxylic acid protecting group (Cbz). The reaction can be carried out using common organic synthesis methods under appropriate reaction conditions.
N-epsilon-cbz-D-lysine safety information is limited, so appropriate laboratory procedures and personal protective measures should be followed when using or handling this compound. It may cause irritation or other adverse reactions to the human body, so it is recommended to use it under suitable experimental conditions and follow relevant safety guidelines.
Please note that the information provided above is for informational purposes only. Reference should also be made to the relevant literature and safety data sheets for specific applications and operations. When using this compound, it is recommended that it be carried out in a suitable laboratory environment and to ensure that laboratory safety procedures are followed.
Last Update：2024-04-09 20:49:11
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