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Browsing Retention Index for different Chemical Structures
Displaying retention index compounds
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RIpred ID
Structure Name
Chemical Structure
Derivatization Type
Base compound Mass
GC Column/Stationary Phase
Retention Index
RI00000226
Deoxycorticosterone,1TMS,isomer#1
Jsmol
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)C
TMS
402.259
Semi standard non polar
3162.3997
RI00000227
Deoxycorticosterone,1TMS,isomer#2
Jsmol
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)C
TMS
402.259
Semi standard non polar
3098.1843
RI00000228
Deoxycorticosterone,1TMS,isomer#3
Jsmol
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)C
TMS
402.259
Semi standard non polar
3107.1309
RI00000229
Deoxycorticosterone,1TMS,isomer#4
Jsmol
C[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO
TMS
402.259
Semi standard non polar
3044.9802
RI00000230
Deoxycorticosterone,1TBDMS,isomer#1
Jsmol
CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
TBDMS
444.306
Semi standard non polar
3429.5967
RI00000231
Deoxycorticosterone,1TBDMS,isomer#2
Jsmol
CC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
TBDMS
444.306
Semi standard non polar
3375.3423
RI00000232
Deoxycorticosterone,1TBDMS,isomer#3
Jsmol
CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
TBDMS
444.306
Semi standard non polar
3347.3076
RI00000233
Deoxycorticosterone,1TBDMS,isomer#4
Jsmol
CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](C(=O)CO)[C@@]3(C)CC[C@@H]12
TBDMS
444.306
Semi standard non polar
3317.3804
RI00000234
Deoxycorticosterone
Jsmol
[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12C
Underivatized
330.2195
Standard polar
3169.1367
RI00000235
Deoxycorticosterone,2TMS,isomer#1
Jsmol
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)C
TMS
474.2985
Standard non polar
3006.939
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Displaying retention index compounds
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