Spectrum Details
NP-MRD ID:NP0152545
Compound name:[(2r,3s,4s,5r,6s)-6-{4-[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy}-3,4,5-trihydroxyoxan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate
Spectrum type:13C NMR Spectrum (1D, 126 MHz, H2O, predicted)
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?JSV
Multiplets 
192.84
166.37
159.17
152.40
148.58
148.00
146.69
145.45
142.60
131.21
131.21
130.69
130.17
128.30
126.43
122.90
119.28
117.98
116.39
116.13
116.13
114.92
114.37
111.07
101.40
76.43
74.06
73.20
70.23
63.49
Peak Assignment Table
Row No.Cluster MidpointNo. PeaksCoupling TypeNo. C'sAtom No.Peak Centers (ppm)
1192.841s1
22
192.84
2166.371s1
2
166.37
3159.171s1
8
159.17
4152.401s1
34
152.40
5148.581s1
29
148.58
6148.001s1
18
148.00
7146.691s1
31
146.69
8145.451s1
4
145.45
9142.601s1
25
142.60
10131.211s1
11
131.21
11131.211s1
6
131.21
12130.691s1
36
130.69
13130.171s1
26
130.17
14128.301s1
20
128.30
15126.431s1
5
126.43
16122.901s1
27
122.90
17119.281s1
21
119.28
18117.981s1
24
117.98
19116.391s1
28
116.39
20116.131s1
10
116.13
21116.131s1
7
116.13
22114.921s1
33
114.92
23114.371s1
3
114.37
24111.071s1
19
111.07
25101.401s1
16
101.40
2676.431s1
40
76.43
2774.061s1
14
74.06
2873.201s1
38
73.20
2970.231s1
42
70.23
3063.491s1
13
63.49
Experimental Conditions
Solvent:H2O
Nucleus:13C
Frequency:500 MHz
Documentation
Document DescriptionDownloadFile Size
Peak List (TXT)Download file1.58 KB
Peak Assignments (TXT)Download file1.06 KB
Spectra Image with Peak AssignmentsNot AvailableNot Available
Raw Spectrum ImageNot AvailableNot Available
nmrML File (NMRML)Download file563 KB
JCAMP-DX File (JDX)Download file154 KB
Raw Free Induction Decay file for spectral processingNot AvailableNot Available
Validation ReportNot AvailableNot Available
References
Not Available