N-(9-芴甲氧羰基)-D-赖氨酸
(2R)-6-ammonio-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoate
CAS: 110990-08-4
Molecular Formula: C21H24N2O4
N-(9-芴甲氧羰基)-D-赖氨酸 - Names and Identifiers
| Name | (2R)-6-ammonio-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoate |
| Synonyms | D-Lys(FMoc) FMOC-D-LYSINE Fmoc-D-Lys-OH FMOC-D-LYS-OH (9H-Fluoren-9-yl)MethOxy]Carbonyl D-Lys-OH N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-lysine N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-LYSINE D-Lysine, N2-[(9H-fluoren-9-ylMethoxy)carbonyl]- N~2~-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-lysine D-lysine, N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]- (2R)-6-ammonio-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoate |
| CAS | 110990-08-4 |
| InChI | InChI=1/C21H24N2O4.ClH/c22-12-6-5-11-19(20(24)25)23-21(26)27-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18;/h1-4,7-10,18-19H,5-6,11-13,22H2,(H,23,26)(H,24,25);1H/t19-;/m1./s1 |
N-(9-芴甲氧羰基)-D-赖氨酸 - Physico-chemical Properties
| Molecular Formula | C21H24N2O4 |
| Molar Mass | 368.43 |
| Density | 1.245 |
| Boling Point | 607.6±55.0 °C(Predicted) |
| pKa | 3.81±0.21(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
N-(9-芴甲氧羰基)-D-赖氨酸 - Introduction
N-(9-fluorenylmethoxycarbonyl)-D-lysine (N-(fluorenylmethyloxycarbonyl)-D-lysine) is an organic compound. It is synthesized by combining a 9-fluorenylmethyl alcohol and carbonyl dimethyl carbamate on the alpha amino group of lysine.
N-(9-fluorenylmethoxycarbonyl)-D-lysine is commonly used in chemical laboratories as an intermediate for the synthesis of peptides, proteins, and other biologically active compounds. It is able to protect the alpha-amino group of lysine, preventing its accidental reaction. In addition, the compound can also be used to study protein structure and function.
The preparation of N-(9-fluorenylmethyloxycarbonyl)-D-lysine generally uses chemical synthesis. First, lysine is reacted with 9-fluorenylmethyl alcohol to form a lysine 9-fluorenyl ester. Carbonyldimethylcarbamate is then added for esterification to produce the final product, N-(9-fluorenylmethoxycarbonyl)-D-lysine.
For safety information, because the safety of the chemical is related to the use and other factors, it is recommended to follow the chemical laboratory safety procedures and use personal protective equipment when using the compound. In addition, the operation should be carried out in a well-ventilated place, and care should be taken to avoid contact with skin and eyes.
Important Note: This article is for reference only. For specific chemical experiment operations and safety information, please refer to relevant chemical literature or consult professional chemists.
N-(9-fluorenylmethoxycarbonyl)-D-lysine is commonly used in chemical laboratories as an intermediate for the synthesis of peptides, proteins, and other biologically active compounds. It is able to protect the alpha-amino group of lysine, preventing its accidental reaction. In addition, the compound can also be used to study protein structure and function.
The preparation of N-(9-fluorenylmethyloxycarbonyl)-D-lysine generally uses chemical synthesis. First, lysine is reacted with 9-fluorenylmethyl alcohol to form a lysine 9-fluorenyl ester. Carbonyldimethylcarbamate is then added for esterification to produce the final product, N-(9-fluorenylmethoxycarbonyl)-D-lysine.
For safety information, because the safety of the chemical is related to the use and other factors, it is recommended to follow the chemical laboratory safety procedures and use personal protective equipment when using the compound. In addition, the operation should be carried out in a well-ventilated place, and care should be taken to avoid contact with skin and eyes.
Important Note: This article is for reference only. For specific chemical experiment operations and safety information, please refer to relevant chemical literature or consult professional chemists.
Last Update：2024-04-09 21:01:54
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