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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11701 - 11725 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01712476ethylsulfenate,1TMS,isomer#1JsmolCCSO[Si](C)(C)CTMS150.0535Semi standard non polar810.2216
RI01712475ethylsulfenate,1TBDMS,isomer#1JsmolCCSO[Si](C)(C)C(C)(C)CTBDMS192.1004Standard non polar1045.1599
RI01712474ethylsulfenate,1TMS,isomer#1JsmolCCSO[Si](C)(C)CTMS150.0535Standard non polar835.6606
RI01712473episterone,1TBDMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Standard polar3660.088
RI01712472episterone,1TBDMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Standard polar3633.9463
RI01712471episterone,1TMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC21C)C(C)CTMS468.3787Standard polar3535.9355
RI01712470episterone,1TMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC21C)C(C)CTMS468.3787Standard polar3513.2883
RI01712469episterone,1TBDMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Semi standard non polar3592.0142
RI01712468episterone,1TBDMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Semi standard non polar3593.9016
RI01712467episterone,1TMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC21C)C(C)CTMS468.3787Semi standard non polar3361.7705
RI01712466episterone,1TMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC21C)C(C)CTMS468.3787Semi standard non polar3351.1377
RI01712465episterone,1TBDMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Standard non polar3411.4504
RI01712464episterone,1TBDMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC21C)C(C)CTBDMS510.4257Standard non polar3354.134
RI01712463episterone,1TMS,isomer#2JsmolC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC21C)C(C)CTMS468.3787Standard non polar3199.166
RI01712462episterone,1TMS,isomer#1JsmolC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC21C)C(C)CTMS468.3787Standard non polar3152.3623
RI01712461dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#55JsmolCC1=C(O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=C(C)C(=O)N([Si](C)(C)C)C3=O)C[C@@H]2O)O[Si](C)(C)C)O1TMS834.2233Standard polar5230.968
RI01712460dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#54JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)C(O[Si](C)(C)C)=C(O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS834.2233Standard polar5236.745
RI01712459dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#53JsmolCC1=C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=C(C)C(=O)N([Si](C)(C)C)C3=O)C[C@@H]2O)O1TMS834.2233Standard polar5518.6685
RI01712458dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#52JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS834.2233Standard polar5501.143
RI01712457dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#51JsmolCC1=C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=C(C)C(=O)N([Si](C)(C)C)C3=O)C[C@@H]2O)O[Si](C)(C)C)O1TMS834.2233Standard polar5484.3804
RI01712456dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#50JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=OTMS834.2233Standard polar5466.676
RI01712455dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#49JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)C(=O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS834.2233Standard polar5021.0786
RI01712454dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#48JsmolCC1=C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=C(C)C(=O)[NH]C3=O)C[C@@H]2O)O[Si](C)(C)C)O1TMS834.2233Standard polar5116.3057
RI01712453dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#47JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS834.2233Standard polar5095.592
RI01712452dTDP-4-dehydro-6-deoxy-beta-L-mannose,4TMS,isomer#46JsmolCC1=C(O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=C(C)C(=O)N([Si](C)(C)C)C3=O)C[C@@H]2O)O1TMS834.2233Standard polar5523.486
Displaying retention index compounds 11701 - 11725 of 1722868 in total