N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER
Fmoc-Asp(OAll)-OH
CAS: 146982-24-3;283170-10-5
Molecular Formula: C22H21NO6
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER - Names and Identifiers
| Name | Fmoc-Asp(OAll)-OH |
| Synonyms | Fmoc-Asp(OAll) FMOC-ASP(OAL)-OH FMOC-ASP(OAI)-OH FMOC-ASP(OALL)-OH Fmoc-Asp(OAll)-OH FMOC-L-ASP(ALL)-OH FMOC-ASP(OALLYL)-OH fmoc-L-aspartic acid 4-allyl ester N-ALPHA-FMOC-L-ASPARTIC ACID BETA-ALLYL ESTER N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-ASPARTIC ACID BETA ALLYL ESTER (2S)-4-allyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-butanoic acid N-[(2-Propen-1-yloxy)carbonyl]-L-aspartic acid 4-(9H-fluoren-9-ylmethyl) ester |
| CAS | 146982-24-3 283170-10-5 |
| InChI | InChI=1/C22H21NO6/c1-2-11-28-20(24)12-19(21(25)26)23-22(27)29-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18-19H,1,11-13H2,(H,23,27)(H,25,26)/t19-/m0/s1 |
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER - Physico-chemical Properties
| Molecular Formula | C22H21NO6 |
| Molar Mass | 395.41 |
| Density | 1.286±0.06 g/cm3(Predicted) |
| Melting Point | 111-115°C |
| Boling Point | 638.5±55.0 °C(Predicted) |
| Flash Point | 339.97°C |
| Water Solubility | Slightly soluble in water. |
| Vapor Presure | 0mmHg at 25°C |
| Appearance | White to off-white free-flowing powder |
| BRN | 6670219 |
| pKa | 3.59±0.23(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.592 |
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER - 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-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-ALLYL ESTER - Introduction
Fmoc-Asp(OAll)-OH, also known as Fmoc-L-aspartic acid fluorene ester. It is an organic compound with the following properties:
1. Properties: Fmoc-L-aspartate fluorene Ester is a white crystalline solid with a relative molecular mass of 414.45. Its melting point is between 85-90 ° C. And it is insoluble in water and more soluble in some organic solvents, such as methanol, dimethylformamide (DMF) and dichloromethane.
2. Use: Fmoc-L-aspartate fluorene Ester is mainly used for solid phase synthesis of peptide or protein synthesis. It can be used to protect the aspartic acid amino or carboxyl groups to prevent unwanted reactions during the synthesis. In addition, due to its fluorene structure, Fmoc-L-aspartate fluorene ester can be used as a chemical fluorescent probe and has biological activity.
3. Preparation method: Fmoc-L-aspartic acid fluorene Ester is usually prepared by chemical synthesis method. The most common method is to first synthesize fluorenol and then react with L-aspartic acid to give Fmoc-L-aspartic acid fluorene ester. Specific synthetic methods include multi-step chemical reactions that require organic synthesis laboratory conditions and chemicals.
4. Safety Information: Fluorene Fmoc-L-aspartate is relatively safe under normal conditions of use and storage. However, as a chemical substance, it may still produce certain volatility and toxicity to human body and environment. Therefore, when using this compound, it is necessary to follow the corresponding safety procedures and pay attention to appropriate personal protective measures.
1. Properties: Fmoc-L-aspartate fluorene Ester is a white crystalline solid with a relative molecular mass of 414.45. Its melting point is between 85-90 ° C. And it is insoluble in water and more soluble in some organic solvents, such as methanol, dimethylformamide (DMF) and dichloromethane.
2. Use: Fmoc-L-aspartate fluorene Ester is mainly used for solid phase synthesis of peptide or protein synthesis. It can be used to protect the aspartic acid amino or carboxyl groups to prevent unwanted reactions during the synthesis. In addition, due to its fluorene structure, Fmoc-L-aspartate fluorene ester can be used as a chemical fluorescent probe and has biological activity.
3. Preparation method: Fmoc-L-aspartic acid fluorene Ester is usually prepared by chemical synthesis method. The most common method is to first synthesize fluorenol and then react with L-aspartic acid to give Fmoc-L-aspartic acid fluorene ester. Specific synthetic methods include multi-step chemical reactions that require organic synthesis laboratory conditions and chemicals.
4. Safety Information: Fluorene Fmoc-L-aspartate is relatively safe under normal conditions of use and storage. However, as a chemical substance, it may still produce certain volatility and toxicity to human body and environment. Therefore, when using this compound, it is necessary to follow the corresponding safety procedures and pay attention to appropriate personal protective measures.
Last Update：2024-04-09 21:04:16
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Product Name: Fmoc-Asp(Oallyl)-OH Visit Supplier Webpage Request for quotationCAS: 146982-24-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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