Spectrum Details
NP-MRD ID:NP0152896
Compound name:5,7-dihydroxy-2-(4-hydroxyphenyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one
Spectrum type:13C NMR Spectrum (1D, 25 MHz, H2O, predicted)
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?JSV
Multiplets 
179.20
161.77
160.49
157.90
157.85
149.87
134.58
131.68
131.68
124.68
122.50
115.77
115.77
106.66
105.40
103.30
99.81
77.78
77.38
75.75
71.79
71.37
71.01
70.98
70.94
61.84
17.72
Peak Assignment Table
Row No.Cluster MidpointNo. PeaksCoupling TypeNo. C'sAtom No.Peak Centers (ppm)
1179.201s1
36
179.20
2161.771s1
30
161.77
3160.491s1
11
160.49
4157.901s1
33
157.90
5157.851s1
7
157.85
6149.871s1
16
149.87
7134.581s1
6
134.58
8131.681s1
14
131.68
9131.681s1
9
131.68
10124.681s1
17
124.68
11122.501s1
8
122.50
12115.771s1
13
115.77
13115.771s1
10
115.77
14106.661s1
19
106.66
15105.401s1
35
105.40
16103.301s1
4
103.30
1799.811s1
32
99.81
1877.781s1
21
77.78
1977.381s1
26
77.38
2075.751s1
28
75.75
2171.791s1
42
71.79
2271.371s1
40
71.37
2371.011s1
2
71.01
2470.981s1
38
70.98
2570.941s1
24
70.94
2661.841s1
22
61.84
2717.721s1
1
17.72
Experimental Conditions
Solvent:H2O
Nucleus:13C
Frequency:100 MHz
Documentation
Document DescriptionDownloadFile Size
Peak List (TXT)Download file1.42 KB
Peak Assignments (TXT)Download file1.06 KB
Spectra Image with Peak AssignmentsNot AvailableNot Available
Raw Spectrum ImageNot AvailableNot Available
nmrML File (NMRML)Download file562 KB
JCAMP-DX File (JDX)Download file158 KB
Raw Free Induction Decay file for spectral processingNot AvailableNot Available
Validation ReportNot AvailableNot Available
References
Not Available