Company Name: |
Bide Pharmatech Ltd.
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Tel: |
400-164-7117 13681763483 |
Email: |
product02@bidepharm.com |
Products Intro: |
Product Name:(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)propanoic acid CAS:133342-64-0 Purity:98% Remarks:BD01374918
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Company Name: |
TCI (Shanghai) Chemical Trading Co., Ltd.
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Tel: |
021-021-61109150 |
Email: |
sales@tcisct.com |
Products Intro: |
Product Name:(S)-N-(9-fluorenylmethoxycarbonyl)-[4-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenyl]alanine CAS:133342-64-0 Package:1KG;10KG;100KG; Remarks: 纯度:根据客户需求提供
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| L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]- Basic information |
Product Name: | L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]- | Synonyms: | L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]-;2-{N-(9-Fluorenylmethoxycarbonyl)-L-amino-3-[4-{3-(trifluoromethyl)-3H-diazirin-3-yl}phenyl]propanoic acid;(S)-N-(9-fluorenylmethoxycarbonyl)-[4-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenyl]alanine;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)propanoic acid | CAS: | 133342-64-0 | MF: | C26H20F3N3O4 | MW: | 495.45 | EINECS: | | Product Categories: | | Mol File: | 133342-64-0.mol | |
| L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]- Chemical Properties |
Melting point | 129-130 °C | density | 1.45±0.1 g/cm3(Predicted) | storage temp. | -20°C | pka | 3.76±0.10(Predicted) |
| L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]- Usage And Synthesis |
Uses | Fmoc-L-Photo-Phe-OH is a diazirine-containing, Fmoc-protected phenylalanine amino acid and multifunctional photo-crosslinker. Its incorporation into peptides or small-molecule probes and tools allows for photoaffinity labeling of cellular targets and protein-protein interactions upon UV light (~360 nm) irradiation to form a covalent bond. This and other multifunctional probe building blocks will continue to accelerate drug discovery research for probing cellular mechanisms, target ID/validation, and understanding traditionally undruggable targets. An unprotected version is also available as 907340. |
| L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]- Preparation Products And Raw materials |
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