Fmoc-ser-ome structure
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Common Name | Fmoc-ser-ome | ||
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CAS Number | 82911-78-2 | Molecular Weight | 341.358 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 579.4±45.0 °C at 760 mmHg | |
Molecular Formula | C19H19NO5 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 304.2±28.7 °C |
Use of Fmoc-ser-omeFmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor[1][2]. |
Name | (S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxypropanoate |
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Synonym | More Synonyms |
Description | Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor[1][2]. |
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Related Catalog | |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 579.4±45.0 °C at 760 mmHg |
Molecular Formula | C19H19NO5 |
Molecular Weight | 341.358 |
Flash Point | 304.2±28.7 °C |
Exact Mass | 341.126312 |
PSA | 88.35000 |
LogP | 3.25 |
Vapour Pressure | 0.0±1.7 mmHg at 25°C |
Index of Refraction | 1.595 |
Storage condition | -15°C |
HS Code | 2924299090 |
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~98% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Shao, Hui; Lockman, Jeffrey W.; Parquette, Jon R. Journal of the American Chemical Society, 2007 , vol. 129, # 7 p. 1884 - 1885 |
~94% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Zhang, Fa; Zhang, Wei; Zhang, Yan; Curran, Dennis P.; Liu, Gang Journal of Organic Chemistry, 2009 , vol. 74, # 6 p. 2594 - 2597 |
~% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Bioorganic and Medicinal Chemistry, , vol. 22, # 4 p. 1421 - 1428 |
~80% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Lapatsanis, Lucas; Milias, George; Froussios, Kleanthis; Kolovos, Miltiadis Synthesis, 1983 , # 8 p. 671 - 673 |
~% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Organic letters, , vol. 3, # 16 p. 2477 - 2479 |
~% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980 |
~% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980 |
~% Fmoc-ser-ome CAS#:82911-78-2 |
Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980 |
Precursor 10 | |
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DownStream 5 | |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, methyl ester |
Methyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]serinate |
methyl (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoate |
Fmoc-Ser-Ome |