Spectrum Details
NP-MRD ID:NP0200473
Compound name:(1r,2r,3as,3bs,7s,9ar,9bs,11as)-9a,11a-dimethyl-1-[(1s)-1-[(2r,5s)-5-methylpiperidin-2-yl]ethyl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-2,7-diol
Spectrum type:1H NMR Spectrum (1D, 800 MHz, H2O, predicted)
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?JSV
Multiplets 
5.31
4.41
3.69
2.99
2.83
2.55
2.44
2.28
2.13
1.86
1.85
1.85
1.84
1.79
1.58
1.54
1.50
1.49
1.49
1.48
1.04
1.04
0.99
0.94
0.89
0.82
Peak Assignment Table
Row No.Cluster MidpointNo. PeaksCoupling TypeNo. H'sAtom No.Peak Centers (ppm)
15.313dd1
53
5.315.315.31
24.4112ddd1
45
4.394.404.404.404.414.414.414.414.424.424.424.43
33.6930m1
56
3.663.663.673.673.673.673.683.683.683.683.683.683.693.693.693.693.693.693.703.703.703.703.703.703.713.713.713.713.723.72
42.996ddd1
39
2.982.982.992.993.003.00
52.8316m1
40
2.812.822.822.822.822.832.832.832.832.832.832.842.842.842.842.85
62.557dd2
74
75
2.542.552.562.532.552.562.57
72.448dd2
54
55
2.432.442.442.452.422.442.442.46
82.289ddd2
47
48
2.252.272.282.292.312.272.282.282.29
92.1328m1
34
2.102.102.102.102.112.112.112.112.122.122.122.122.132.132.132.132.132.142.142.142.152.152.152.152.162.162.162.16
101.864dd1
44
1.851.861.861.87
111.8514ddd1
59
1.821.831.831.841.851.851.851.851.851.851.861.871.881.88
121.8518m1
58
1.821.831.841.841.841.841.841.851.851.851.851.861.861.861.861.861.871.88
131.8445m2
37
38
1.801.811.821.821.831.831.831.831.841.841.841.851.851.851.851.851.851.861.861.871.881.801.811.811.821.821.821.831.831.831.841.841.841.841.851.851.851.851.861.861.861.861.871.871.88
141.7912ddd2
51
52
1.771.781.791.791.801.811.771.781.791.791.801.81
151.5837m2
35
36
1.551.551.561.561.561.561.571.571.581.581.581.581.591.591.601.601.601.601.601.601.611.611.551.571.571.571.571.581.581.581.581.581.591.591.591.601.61
161.5417m1
50
1.501.511.531.531.531.531.541.541.541.541.541.541.551.551.551.551.57
171.5039m2
66
67
1.471.471.491.491.491.491.501.501.501.501.501.511.511.511.511.521.531.461.481.481.481.491.491.491.491.501.501.501.501.511.511.511.521.521.521.521.531.531.54
181.4912dd1
61
1.461.471.481.481.481.491.491.501.501.501.511.52
191.4916ddd1
60
1.461.471.471.471.481.481.481.491.491.491.501.501.511.511.511.52
201.4836ddd2
68
69
1.451.461.461.461.471.471.471.481.481.481.491.491.501.501.501.511.521.441.451.461.461.471.471.471.481.481.481.481.481.481.491.491.491.501.501.51
211.042d3
41
42
43
1.041.04
221.0412ddd1
49
1.021.021.031.031.031.041.041.051.051.051.061.06
230.991s3
62
63
64
0.99
240.9446ddd1
65
0.890.900.900.900.900.910.910.910.910.910.920.920.920.920.920.920.930.930.930.930.930.940.940.940.940.940.940.950.950.950.950.950.950.960.960.960.960.970.970.970.970.980.980.980.990.99
250.891s3
70
71
72
0.89
260.823t3
31
32
33
0.830.820.82
Experimental Conditions
Solvent:H2O
Nucleus:1H
Frequency:800 MHz
Documentation
Document DescriptionDownloadFile Size
Peak List (TXT)Download file23.9 KB
Peak Assignments (TXT)Download file1.31 KB
Spectra Image with Peak AssignmentsNot AvailableNot Available
Raw Spectrum ImageNot AvailableNot Available
nmrML File (NMRML)Download file596 KB
JCAMP-DX File (JDX)Download file184 KB
Raw Free Induction Decay file for spectral processingNot AvailableNot Available
Validation ReportNot AvailableNot Available
References
Not Available