The Fmoc-L-Serine is an organic compound with the formula C₁₈H₁₇NO₅. The IUPAC name of this chemical is (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoate. With the CAS registry number 73724-45-5, it is also named as L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-. The product's categories are Protected Amino Acids; Amino Acids; Serine [Ser, S]; Fmoc-Amino Acids and Derivatives; Amino Acids (N-Protected); Biochemistry; Fmoc-Amino Acids; Fmoc-Amino Acid Series. Besides, it should be stored in a closed cool and dry place.

Physical properties about Fmoc-L-Serine are: (1)ACD/LogP: 2.66; (2)ACD/LogD (pH 5.5): 0.21; (3)ACD/LogD (pH 7.4): -1; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 2.35; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 6; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 7; (11)Polar Surface Area: 65.07 Å²; (12)Index of Refraction: 1.629; (13)Molar Refractivity: 85.44 cm³; (14)Molar Volume: 240.2 cm³; (15)Polarizability: 33.87×10^-24cm³; (16)Surface Tension: 63.7 dyne/cm; (17)Density: 1.362 g/cm³; (18)Flash Point: 316.2 °C; (19)Enthalpy of Vaporization: 93.83 kJ/mol; (20)Boiling Point: 599.3 °C at 760 mmHg; (21)Vapour Pressure: 3.27E-15 mmHg at 25°C.

Preparation: this chemical can be prepared by O-(tert-butyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine. This reaction will need reagent Et₃SiH, CF₃CO₂H and solvent CH₂Cl₂. The reaction time is 15 min at ambient temperature. The yield is about 99%.

Uses of Fmoc-L-Serine: it can be used to produce (S)-3-[(9-Fluorenyl)methoxycarbamoyl]oxeatn-2-one. It will need reagent PPh₃, dimethyl azodicarboxylate. The yield is about 73%.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, do not breathe dust and avoid contact with skin and eyes. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(O)[C@@H](NC(=O)OCC3c1ccccc1c2c3cccc2)CO
(2)InChI: InChI=1/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
(3)InChIKey: JZTKZVJMSCONAK-INIZCTEOBO
(4)Std. 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
(5)Std. InChIKey: JZTKZVJMSCONAK-INIZCTEOSA-N