Boc-Cha-OH H2O
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Boc-Cha-OH H2O

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Category
BOC-Amino Acids
Catalog number
BAT-000983
CAS number
349560-47-0
Molecular Formula
C14H27NO5
Molecular Weight
289.37
IUPAC Name
(2S)-3-cyclohexyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;hydrate
Synonyms
Boc-Phe(hexahydro)-OH H2O; Boc-3-cyclohexyl-L-alanine hydrate; N-α-(t-Butoxycarbonyl)-β-cyclohexyl-L-alanine hydrate; N-α-(t-Butoxycarbonyl)-hexahydro-L-phenylalanine hydrate; (2S)-3-cyclohexyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid hydrate
Storage
Store at 2-8 °C
InChI
InChI=1S/C14H25NO4.H2O/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10;/h10-11H,4-9H2,1-3H3,(H,15,18)(H,16,17);1H2/t11-;/m0./s1
InChI Key
KGIDHDHQFLWAMT-MERQFXBCSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1CCCCC1)C(=O)O.O
1. Infrared spectra of the OH+ and H2O+ cations solvated in solid argon
Han Zhou, Rongjing Yang, Xi Jin, Mingfei Zhou J Phys Chem A. 2005 Jul 14;109(27):6003-7. doi: 10.1021/jp0511808.
Infrared spectra of various OH+ and H2O+ isotopomers solvated in solid argon are presented. The OH+ and H2O+ cations were produced by co-deposition of H2O/Ar mixture with high-frequency discharged Ar at 4 K. Detailed isotopic substitution studies confirm the assignments of absorptions at 3054.9 and 3040.0 cm(-1) to the antisymmetric and symmetric H-O-H stretching vibrations of H2O+ and 2979.6 cm(-1) to the O-H stretching vibration of OH+. The frequencies of H2O+ solvated in solid argon are red-shifted, whereas the frequency of OH+ is blue-shifted with respect to the gas-phase fundamentals. On the basis of previous gas-phase studies and quantum chemical calculations, the OH+ and H2O+ cations solvated in solid argon may be regarded as the OH+-Ar5 and H2O+-Ar4 complexes isolated in the argon matrix.
2. Individualized versus Fixed Positive End-expiratory Pressure for Intraoperative Mechanical Ventilation in Obese Patients: A Secondary Analysis
Philipp Simon, et al. Anesthesiology. 2021 Jun 1;134(6):887-900. doi: 10.1097/ALN.0000000000003762.
Background: General anesthesia may cause atelectasis and deterioration in oxygenation in obese patients. The authors hypothesized that individualized positive end-expiratory pressure (PEEP) improves intraoperative oxygenation and ventilation distribution compared to fixed PEEP. Methods: This secondary analysis included all obese patients recruited at University Hospital of Leipzig from the multicenter Protective Intraoperative Ventilation with Higher versus Lower Levels of Positive End-Expiratory Pressure in Obese Patients (PROBESE) trial (n = 42) and likewise all obese patients from a local single-center trial (n = 54). Inclusion criteria for both trials were elective laparoscopic abdominal surgery, body mass index greater than or equal to 35 kg/m2, and Assess Respiratory Risk in Surgical Patients in Catalonia (ARISCAT) score greater than or equal to 26. Patients were randomized to PEEP of 4 cm H2O (n = 19) or a recruitment maneuver followed by PEEP of 12 cm H2O (n = 21) in the PROBESE study. In the single-center study, they were randomized to PEEP of 5 cm H2O (n = 25) or a recruitment maneuver followed by individualized PEEP (n = 25) determined by electrical impedance tomography. Primary endpoint was Pao2/inspiratory oxygen fraction before extubation and secondary endpoints included intraoperative tidal volume distribution to dependent lung and driving pressure. Results: Ninety patients were evaluated in three groups after combining the two lower PEEP groups. Median individualized PEEP was 18 (interquartile range, 16 to 22; range, 10 to 26) cm H2O. Pao2/inspiratory oxygen fraction before extubation was 515 (individual PEEP), 370 (fixed PEEP of 12 cm H2O), and 305 (fixed PEEP of 4 to 5 cm H2O) mmHg (difference to individualized PEEP, 145; 95% CI, 91 to 200; P < 0.001 for fixed PEEP of 12 cm H2O and 210; 95% CI, 164 to 257; P < 0.001 for fixed PEEP of 4 to 5 cm H2O). Intraoperative tidal volume in the dependent lung areas was 43.9% (individualized PEEP), 25.9% (fixed PEEP of 12 cm H2O) and 26.8% (fixed PEEP of 4 to 5 cm H2O) (difference to individualized PEEP: 18.0%; 95% CI, 8.0 to 20.7; P < 0.001 for fixed PEEP of 12 cm H2O and 17.1%; 95% CI, 10.0 to 20.6; P < 0.001 for fixed PEEP of 4 to 5 cm H2O). Mean intraoperative driving pressure was 9.8 cm H2O (individualized PEEP), 14.4 cm H2O (fixed PEEP of 12 cm H2O), and 18.8 cm H2O (fixed PEEP of 4 to 5 cm H2O), P < 0.001. Conclusions: This secondary analysis of obese patients undergoing laparoscopic surgery found better oxygenation, lower driving pressures, and redistribution of ventilation toward dependent lung areas measured by electrical impedance tomography using individualized PEEP. The impact on patient outcome remains unclear.
3. I + (H2O)2 → HI + (H2O)OH Forward and Reverse Reactions. CCSD(T) Studies Including Spin-Orbit Coupling
Hui Wang, Guoliang Li, Qian-Shu Li, Yaoming Xie, Henry F Schaefer 3rd J Phys Chem B. 2016 Mar 3;120(8):1743-8. doi: 10.1021/acs.jpcb.5b09253. Epub 2015 Nov 25.
The potential energy profile for the atomic iodine plus water dimer reaction I + (H2O)2 → HI + (H2O)OH has been explored using the "Gold Standard" CCSD(T) method with quadruple-ζ correlation-consistent basis sets. The corresponding information for the reverse reaction HI + (H2O)OH → I + (H2O)2 is also derived. Both zero-point vibrational energies (ZPVEs) and spin-orbit (SO) coupling are considered, and these notably alter the classical energetics. On the basis of the CCSD(T)/cc-pVQZ-PP results, including ZPVE and SO coupling, the forward reaction is found to be endothermic by 47.4 kcal/mol, implying a significant exothermicity for the reverse reaction. The entrance complex I···(H2O)2 is bound by 1.8 kcal/mol, and this dissociation energy is significantly affected by SO coupling. The reaction barrier lies 45.1 kcal/mol higher than the reactants. The exit complex HI···(H2O)OH is bound by 3.0 kcal/mol relative to the asymptotic limit. At every level of theory, the reverse reaction HI + (H2O)OH → I + (H2O)2 proceeds without a barrier. Compared with the analogous water monomer reaction I + H2O → HI + OH, the additional water molecule reduces the relative energies of the entrance stationary point, transition state, and exit complex by 3-5 kcal/mol. The I + (H2O)2 reaction is related to the valence isoelectronic bromine and chlorine reactions but is distinctly different from the F + (H2O)2 system.
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