The Lysine,N2,N6-bis[(phenylmethoxy)carbonyl]-, with the CAS registry number 55592-85-3, has the systematic name of N²,N⁶-bis[(benzyloxy)carbonyl]lysine. And the molecular formula of the chemical is C₂₂H₂₆N₂O₆. What's more, while dealing with this chemical, you should not breathe dust and then try to avoid contacting with skin and eyes.

The characteristics of Lysine,N2,N6-bis[(phenylmethoxy)carbonyl]- are as followings: (1)ACD/LogP: 3.75; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.79; (4)ACD/LogD (pH 7.4): 0.25; (5)ACD/BCF (pH 5.5): 4.58; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 28.72; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 8; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 13; (12)olar Surface Area: 85.38 Å²; (13)Index of Refraction: 1.568; (14)Molar Refractivity: 109.61 cm³; (15)Molar Volume: 334.6 cm³; (16)Polarizability: 43.45×10^-24cm³; (17)Surface Tension: 52 dyne/cm; (18)Density: 1.238 g/cm³; (19)Flash Point: 352.4 °C; (20)Enthalpy of Vaporization: 101.91 kJ/mol; (21)Boiling Point: 659 °C at 760 mmHg; (22)Vapour Pressure: 2.9E-18 mmHg at 25°C.

Uses of Lysine,N2,N6-bis[(phenylmethoxy)carbonyl]-: It can react with 5-amino-1H-[1,2,3]triazole-4-carboxylic acid amide to produce [5-benzyloxycarbonylamino-5-(5-carbamoyl-3H-[1,2,3]triazol-4-ylcarbamoyl)-pentyl]-carbamic acid benzyl ester. This reaction will need reagent N,N'-carbonyldiimidazole, and the yield is about 45%.   

Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: O=C(O)C(NC(=O)OCc1ccccc1)CCCCNC(=O)OCc2ccccc2
(2)InChI: InChI=1/C22H26N2O6/c25-20(26)19(24-22(28)30-16-18-11-5-2-6-12-18)13-7-8-14-23-21(27)29-15-17-9-3-1-4-10-17/h1-6,9-12,19H,7-8,13-16H2,(H,23,27)(H,24,28)(H,25,26)
(3)InChIKey: BLZXFNUZFTZCFD-UHFFFAOYAP