N-FMOC-3-硝基-L-酪氨酸 - Names and Identifiers
Name | fmoc-3-nitro-L-tyrosine
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Synonyms | FMOC-TYR(3-NO2)-OH Fmoc-Tyr(3-NO2)-OH Fmoc-3-nitro-Tyr-OH FMOC-M-NITRO-TYR-OH FMOC-L-TYR(3-NO2)-OH fmoc-3-nitro-L-tyrosine FMOC-PHE(P-OH,M-NO2)-OH FMOC-M-NITRO-P-HYDROXY-PHE-OH N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-nitrotyrosine N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-nitro-L-tyrosine N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-3-NITROTYROSINE N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-(S)-2-AMINO-3-(M-NITRO-P-HYDROXY) PHENYLPROPANOIC ACID 2-[[(2-ethylidene-3-prop-2-enylidene-1H-inden-1-yl)methoxy-oxomethyl]amino]-3-(4-hydroxy-3-nitrophenyl)propanoic acid
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CAS | 136590-09-5
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EINECS | 000-000-0 |
InChI | InChI=1/C24H20N2O7/c27-22-10-9-14(12-21(22)26(31)32)11-20(23(28)29)25-24(30)33-13-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-10,12,19-20,27H,11,13H2,(H,25,30)(H,28,29) |
N-FMOC-3-硝基-L-酪氨酸 - Physico-chemical Properties
Molecular Formula | C24H20N2O7
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Molar Mass | 448.42 |
Density | 1.429±0.06 g/cm3(Predicted) |
Boling Point | 704.4±60.0 °C(Predicted) |
Flash Point | 379.8°C |
Vapor Presure | 7.97E-21mmHg at 25°C |
pKa | 2.77±0.10(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Refractive Index | 1.667 |
MDL | MFCD00171383 |
N-FMOC-3-硝基-L-酪氨酸 - Risk and Safety
Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
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WGK Germany | 3 |
HS Code | 29242990 |
Hazard Class | IRRITANT |
N-FMOC-3-硝基-L-酪氨酸 - Introduction
Fmoc-3-nitro-L-tyrosine (Fmoc-3-nitro-L-tyrosine) is an organic compound with the molecular formula C28H20N2O7 and a relative molecular mass of 492.47.
In terms of properties, Fmoc-3-nitro-L-tyrosine is a yellow crystalline powder. It has excellent stability and light resistance, and can be synthesized under oxidizing conditions, but it is more sensitive to acids and alkalis.
Fmoc-3-nitro-L-tyrosine is mainly used in biochemistry and ligand design. It can be used as a synthetic intermediate for fluorescent probes, functional molecules and antibacterial agents. In addition, it can also be used for the synthesis of biologically active peptides or proteins.
Preparation method, the preparation of Fmoc-3-nitro-L-tyrosine can be achieved by a variety of methods. One commonly used method is the esterification reaction using an Fmoc protecting group and 3-nitro-L-tyrosine.
For safety information, Fmoc-3-nitro-L-tyrosine needs to be stored in the dark and avoid contact with oxygen, acids and bases. During use, it is necessary to wear appropriate protective equipment, such as laboratory gloves, eye protection, etc. In addition, information on its specific toxicity and risk needs to be evaluated and understood in detail on a case-by-case basis.
Last Update:2024-04-10 22:30:50