N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE
N(alpha)-fmoc-N(epsilon)-alloc-L-lysine
CAS: 146982-27-6
Molecular Formula: C25H28N2O6
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE - Names and Identifiers
| Name | N(alpha)-fmoc-N(epsilon)-alloc-L-lysine |
| Synonyms | FMOC-LYS(ALOC)-OH Fmoc-Lys(Aloc)-OH FMOC-LYS(ALLOC)-OH Fmoc-Lys(Alloc)-OH FMOC-LYSINE(ALOC)-OH FMOC-L-LYS(ALLOC)-OH N-ALPHA-FMOC-N-EPSILON-ALLOC-L-LYSINE N(alpha)-fmoc-N(epsilon)-alloc-L-lysine N-ALPHA-FMOC-N-EPSILON-ALLYLOXYCARBONYL-L-LYSINE N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-ALLYLOXYCARBONYL-L-LYSINE N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]-N~6~-[(prop-2-en-1-yloxy)carbonyl]-L-lysine |
| CAS | 146982-27-6 |
| InChI | InChI=1/C25H28N2O6/c1-2-15-32-24(30)26-14-8-7-13-22(23(28)29)27-25(31)33-16-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-6,9-12,21-22H,1,7-8,13-16H2,(H,26,30)(H,27,31)(H,28,29)/t22-/m0/s1 |
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE - Physico-chemical Properties
| Molecular Formula | C25H28N2O6 |
| Molar Mass | 452.5 |
| Density | 1.237±0.06 g/cm3(Predicted) |
| Melting Point | 87-91°C |
| Boling Point | 689.7±55.0 °C(Predicted) |
| Flash Point | 370.917°C |
| Vapor Presure | 0mmHg at 25°C |
| Appearance | Light brown powder |
| BRN | 5893081 |
| pKa | 3.88±0.21(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.579 |
| MDL | MFCD00016339 |
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 2924 29 70 |
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-ALLYL-OXYCARBONYL-L-LYSINE - Introduction
N(alpha)-fmoc-N(epsilon)-alloc-L-lysine (English name: N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N'-[(2-propenyloxy)carbonyl]-L-lysine) it is a complex organic compound.
Nature:
The compound is a powdery substance having a white or off-white solid. It has high solubility in dissolving agents and can be dissolved in common solvents such as water, methanol, ethanol and dichloromethane. Its molecular formula is C23H25N3O5, the relative molecular mass is 423.47g/mol.
Use:
N(alpha)-fmoc-N(epsilon)-alloc-L-lysine is an important organic synthesis intermediate. It is commonly used in the synthesis of peptides, proteins and drugs, can be used as a protecting group or reactive group.
Method:
The preparation method of N(alpha)-fmoc-N(epsilon)-alloc-L-lysine is relatively complicated and requires multiple reactions. One common method of preparation is by the reaction of aminolytic addition. Specific steps can be carried out with reference to the relevant organic synthesis literature.
Safety Information:
There are no publicly available details regarding the safety of this compound. However, because it is an organic compound and has certain chemical reactivity, it is recommended to pay attention to follow laboratory safety procedures and personal protective measures during use, storage and handling. During the operation, wear appropriate protective gloves, protective glasses and laboratory goggles, and ensure that the operating environment is well ventilated. If you intend to come into contact with this compound, please refer to the safety instructions in the relevant literature and seek professional assistance if necessary.
Nature:
The compound is a powdery substance having a white or off-white solid. It has high solubility in dissolving agents and can be dissolved in common solvents such as water, methanol, ethanol and dichloromethane. Its molecular formula is C23H25N3O5, the relative molecular mass is 423.47g/mol.
Use:
N(alpha)-fmoc-N(epsilon)-alloc-L-lysine is an important organic synthesis intermediate. It is commonly used in the synthesis of peptides, proteins and drugs, can be used as a protecting group or reactive group.
Method:
The preparation method of N(alpha)-fmoc-N(epsilon)-alloc-L-lysine is relatively complicated and requires multiple reactions. One common method of preparation is by the reaction of aminolytic addition. Specific steps can be carried out with reference to the relevant organic synthesis literature.
Safety Information:
There are no publicly available details regarding the safety of this compound. However, because it is an organic compound and has certain chemical reactivity, it is recommended to pay attention to follow laboratory safety procedures and personal protective measures during use, storage and handling. During the operation, wear appropriate protective gloves, protective glasses and laboratory goggles, and ensure that the operating environment is well ventilated. If you intend to come into contact with this compound, please refer to the safety instructions in the relevant literature and seek professional assistance if necessary.
Last Update：2024-04-09 21:54:55
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Product Name: Fmoc-Lys(Alloc)-OH Visit Supplier Webpage Request for quotationCAS: 146982-27-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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