Nalpha-FMOC-L-Tryptophan
- Name Nalpha-FMOC-L-Tryptophan
- CAS 35737-15-6
- Purity 99%
Product Details
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What is the Nalpha-FMOC-L-Tryptophan ?
Nalpha-FMOC-L-Tryptophan is white to off-white crystalline powder, while it's Molecular Formula is C26H22N2O4. Nα-Fmoc-L-tryptophan is an N-Fmoc protected form of L-Tryptophan (T947210). L-Tryptophan is an essential amino acid that is important for cell proliferation and the biosynthesis of proteins. It is a precursor to Serotonin (HCl: S274980), a neurotransmitter that compound that aids in sleep and mental state. L-Tryptophan is also thought to cause eosinophilia-myalgia syndrome.
What is the CAS number for Nalpha-FMOC-L-Tryptophan ?
The CAS number of Nalpha-FMOC-L-Tryptophan is 35737-15-6.
More information of Nalpha-FMOC-L-Tryptophan 35737-15-6 are:
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Synonyms |
L-Tryptophan,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-;(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-3-(1H-indol-3-yl)propionicacid;FMOC-Trp-OH;Fmoc-tryptophan;N-(9-Fluorenylmethoxycarbonyl)tryptophan;N-(Fluorenyl-9-methoxycarbonyl)-terminated tryptophan;NSC 334295; |
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CAS?Number |
35737-15-6 |
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Molecular Formula |
C26H22N2O4 |
|
Molecular Weight |
426.472 |
|
Density |
1.35 g/cm3 |
|
Melting Point |
183-185 °C |
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Boiling Point |
711.9 °C at 760 mmHg |
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Flash Point |
384.3 °C |
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HS CODE |
2933 99 80 |
|
PSA |
91.42000 |
|
LogP |
5.09320 |
|
Pka |
3.89±0.10(Predicted) |
What is Nalpha-FMOC-L-Tryptophan (35737-15-6) used for?
Nalpha-FMOC-L-Tryptophan, also known as N-Fmoc protected form of L-Tryptophan, is an essential amino acid derivative that plays a crucial role in cell proliferation and protein biosynthesis. It serves as a precursor to Serotonin, a neurotransmitter that helps regulate sleep and mental state. Additionally, L-Tryptophan has been linked to eosinophilia-myalgia syndrome. Nalpha-FMOC-L-Tryptophan is characterized by its white to light yellow crystal powder appearance.
InChI:InChI=1/C26H22N2O4/c29-25(30)24(13-16-14-27-23-12-6-5-7-17(16)23)28-26(31)32-15-22-20-10-3-1-8-18(20)19-9-2-4-11-21(19)22/h1-12,14,22,24,27H,13,15H2,(H,28,31)(H,29,30)/p-1/t24-/m0/s1
Articles related to Nalpha-FMOC-L-Tryptophan:
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Article |
Source |
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Fungal Dioxygenase AsqJ Is Promiscuous and Bimodal: Substrate-Directed Formation of Quinolones versus Quinazolinones |
Einsiedler, Manuel,Jamieson, Cooper S.,Maskeri, Mark A.,Houk, Kendall N.,Gulder, Tobias A. M. supporting information, p. 8297 - 8302 (2021/03/01) |
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A facile approach to tryptophan derivatives for the total synthesis of argyrin analogues |
Chen, Chou-Hsiung,Genapathy, Sivaneswary,Fischer, Peter M.,Chan, Weng C. supporting information, p. 9764 - 9768 (2015/01/09) |
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