Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 251 - 275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00000251Deoxycorticosterone,2TMS,isomer#1JsmolC[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)CTMS474.2985Semi standard non polar3155.0718
RI00000252Deoxycorticosterone,2TMS,isomer#2JsmolC[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[Si](C)(C)CTMS474.2985Semi standard non polar3077.2097
RI00000253Deoxycorticosterone,2TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS474.2985Semi standard non polar3196.141
RI00000254Deoxycorticosterone,2TMS,isomer#4JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS474.2985Semi standard non polar3063.1653
RI00000255Deoxycorticosterone,2TMS,isomer#5JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS474.2985Semi standard non polar3041.5266
RI00000256Deoxycorticosterone,3TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS546.3381Semi standard non polar3108.8057
RI00000257Deoxycorticosterone,3TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS546.3381Semi standard non polar3110.4646
RI00000258Deoxycorticosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Semi standard non polar3689.8906
RI00000259Deoxycorticosterone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Semi standard non polar3665.8857
RI00000260Deoxycorticosterone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Semi standard non polar3599.93
RI00000261Deoxycorticosterone,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CCC(=C(CO)O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS558.3924Semi standard non polar3599.7837
RI00000262Deoxycorticosterone,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS558.3924Semi standard non polar3541.2183
RI00000263Deoxycorticosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS672.4789Semi standard non polar3849.7908
RI00000264Deoxycorticosterone,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS672.4789Semi standard non polar3822.2168
RI00000265Deoxycorticosterone,2TMS,isomer#1JsmolC[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)CTMS474.2985Standard polar3423.365
RI00000266Deoxycorticosterone,2TMS,isomer#2JsmolC[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[Si](C)(C)CTMS474.2985Standard polar3433.5322
RI00000267Deoxycorticosterone,2TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS474.2985Standard polar3421.9158
RI00000268Deoxycorticosterone,2TMS,isomer#4JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS474.2985Standard polar3443.8296
RI00000269Deoxycorticosterone,2TMS,isomer#5JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS474.2985Standard polar3458.9705
RI00000270Deoxycorticosterone,3TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS546.3381Standard polar3405.0696
RI00000271Deoxycorticosterone,3TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS546.3381Standard polar3422.715
RI00000272Deoxycorticosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Standard polar3637.9204
RI00000273Deoxycorticosterone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Standard polar3648.2017
RI00000274Deoxycorticosterone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS558.3924Standard polar3647.3308
RI00000275Deoxycorticosterone,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CCC(=C(CO)O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS558.3924Standard polar3667.5437
Displaying retention index compounds 251 - 275 of 1722868 in total