| Identification | More | [Name]
Fmoc-L-Serine | [CAS]
73724-45-5 | [Synonyms]
FMOC-L-SERINE
FMOC-L-SER-OH
FMOC-SERINE
FMOC-SER-OH
N-(9-FLUORENYLMETHOXYCARBONYL)-L-SERINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-SERINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-SERINE
N-ALPHA-FMOC-L-SERINE
N-FMOC-L-SERINE
N-(9-Fluorenylmethoxycarbonyl)-L-serine~Fmoc-Ser-OH
N-Fmoc-L-serine monohydrate
FMOC-L-SERINE, 98+%
n-[(9h-fluoren-9-ylmethoxy)carbonyl]-l-serine
FMOC-SER
FMOC-L-SERINE extrapure
N-(9-Fluorenylmethoxycarbonyl)-L-serine ,99% | [EINECS(EC#)]
690-938-2 | [Molecular Formula]
C18H17NO5 | [MDL Number]
MFCD00051928 | [Molecular Weight]
327.33 | [MOL File]
73724-45-5.mol |
| Chemical Properties | Back Directory | [Melting point ]
104-106°C | [alpha ]
-12.5 º (c=1%, DMF) | [Boiling point ]
599.3±50.0 °C(Predicted) | [density ]
1.362±0.06 g/cm3(Predicted) | [refractive index ]
-12.5 ° (C=1, DMF) | [storage temp. ]
2-8°C
| [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
3.51±0.10(Predicted) | [color ]
White to Light yellow | [optical activity]
[α]20/D 12.5±1°, c = 1% in DMF | [Detection Methods]
T,NMR,Rotation | [BRN ]
4715791 | [InChI]
InChI=1S/C18H17NO5/c20-9-16(17(21)22)19-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16,20H,9-10H2,(H,19,23)(H,21,22)/t16-/m0/s1 | [InChIKey]
JZTKZVJMSCONAK-INIZCTEOSA-N | [SMILES]
C(O)(=O)[C@H](CO)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O | [CAS DataBase Reference]
73724-45-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HS Code ]
29242990 |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow powder | [Uses]
N-Fmoc-L-serine is an N-Fmoc-protected form of L-Serine (S270975). L-Serine is a nonessential amino acid that is required for the synthesis of sphingolipids and phosphatidylserine, compounds that are important for central nervous system neuronal survival. L-Serine is also important in intermediary metabolism in eukaryotic cells. |
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