/ Absolute Configuration Determination (NMR);Enantiomer Excess & Absolute Configuration Determination;for Resolution of Acids;Optical Resolution;Synthetic Organic Chemistry;Chiral Compound;Benzene derivatives;3886-69-9 Mol File: 3886-69-9.mol(R)-(+)-1-Phenylethylamine Chemical Properties...
(±)-1-Phenylethylamine: 1 H NMR (CDCl 3 , 200 MHz) δ 1.37 (d, J =6.4 Hz, 3H), 4.07 (q, J =6.7 Hz, 1H), 7.19–7.33 (m, 5H); 13 C NMR (CDCl 3 , 50.29 MHz) δ 25.2 (q), 50.8 (d), 125.2 (d), 126.3 (d), 127.9 (d), 147.3 (s). Preparative Methods: ...
Capot Chemical CAS# 3886-69-9, (R)-(+)-1-Phenylethylamine . 3886-69-9 MSDS,ROS,3886-69-9 MOA,COA,SPECS,pecifications,1H-NMR,GHS,CAT #6060;D-alpha-Phenylethylamine; R-(+)-alpha-Methylbenzylamine; D(+)-alpha-Methylbenzylamine; (+)-PEA; (R)-(+)-1-Phenylethy
10277-86-8 Basic Information Chemical Name(R)-1-phenylethylamine hydrochloride CAS No.10277-86-8 Molecular FormulaC8H12ClN Molecular Weight157.64 PSA26.02000 LogP3.20860 View More10277-86-8 Properties 10277-86-8 Synthesis Route 13437-79-1 2 Suppliers 10277-86-8 17279-30-0 1 Suppliers ...
1,2-DIPHENYLETHYLAMINE(25611-78-3)Raman Atlas of Related Products 1,2-DIPHENYLETHYLAMINE(25611-78-3)1HNMR 1,2-DIPHENYLETHYLAMINE(25611-78-3)13CNMR 1,2-DIPHENYLETHYLAMINE(25611-78-3)MS 1,2-DIPHENYLETHYLAMINE(25611-78-3)IR1 1,2-DIPHENYLETHYLAMINE(25611-78-3)Raman More ...
/ Absolute Configuration Determination (NMR);Enantiomer Excess & Absolute Configuration Determination;for Resolution of Acids;Optical Resolution;Synthetic Organic Chemistry;Chiral Compound;Amines;Aromatics;Chiral Reagents Canonical SMILES: CC(C1=CC=CC=C1)N InChI: InChI=1S/C8H11N/c1-7(9)8-5-3-2-...
The diastereomeric non-equivalence of the 19F \\{NMR\\} signals (0.05–0.09 ppm) of these amides permits use of these derivatives for determination of enantiomeric purity of alpha—substituted acids. The potential for configurational correlations is discussed....
The chelate nature of the P,N ligands in these salts is indicated by their NMR spectra in solution and is confirmed by the crystal structures of (R,RR)-7a and (S,RR)-7a. With the exception of (S,RR)-7a, the complexes 7a and 7b are shown to catalyse the asymmetric hydrogenation of...
Chiral derivatives of 2,4,5,6-tetrachloro-1,3-dicyanobenzene 1 with one, two and three (R)-1-phenylethylamino ((R)-PEA) units 2–4 are prepared and their chiroptical and conformational properties discussed on the bases of the UV/CD, NMR and MM2 data. High polarity of the per...
Crystal structures and NMR data reveal, that the sterically highly congested "tris" salt - with formal C3 symmetry, albeit unsymmetrical in the crystal - constitutes an intriguing structure with two rotamers present in solution.Castiglia, A.El Sehrawi, H.M.Orbegozo, T.Spitzner, D.Claasen, B...