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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)