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Table 2 The observed 1H and 13C NMR spectra data in CDCl3 with a drop of methanol-d 4 at 400 and 100.06 MHz, respectively

From: Structure elucidation of β-sitosterol with antibacterial activity from the root bark of Malva parviflora

Position Type Chemical Shift, δ (ppm) value
13C NMR 1H NMR (multiplicity)
1 CH2 37.28 1.46 (m)
2 CH2 31.69 1.56 (m)
3 CH(OH) 71.82 3.54 (m)
4 CH2 42.33 2.32 (m)
5 QC(=) 140.77
6 CH(=) 121.73 5.37 (overlapping, t)
7 CH2 31.93 2.04 (m)
8 CH 31.93 1.69 (m)
9 CH 50.16 1.55 (m)
10 QC 36.51
11 CH2 21.11 1.52 (m)
12 CH2 39.80 1.51 (m)
13 QC 42.34
14 CH 56.79 1.50 (m)
15 CH2 24.33 1.58 (m)
16 CH2 28.27 1.85 (m)
17 CH 56.08 1.45 (m)
18 CH3 11.89 0.70 (s)
19 CH3 19.42 1.03 (s)
20 CH 36.17 1.60 (m)
21 CH3 18.84 0.94 (overlapping, d)
22 CH2 33.98 0.93 (m)
23 CH2 26.11 1.15 (m)
24 CH 45.86 1.38 (m)
25 CH 29.19 1.57 (m)
26 CH3 19.84 0.84 (overlapping, d)
27 CH3 19.06 0.86 (d)
28 CH2 23.10 1.10 (m)
29 CH3 12.01 0.82 (overlapping, t)
OH 1.98 (s)