RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 66951 - 66975 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000669515-Thymidylic acid,3TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS664.316Standard non polar3486.4688
RI000669525-Thymidylic acid,3TBDMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Standard non polar3503.5686
RI000669535-Thymidylic acid,3TBDMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Standard non polar3484.376
RI000669545-Thymidylic acid,4TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS778.4025Standard non polar3627.3064
RI000669555-Thymidylic acidJsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=OUnderivatized322.0566Semi standard non polar2996.923
RI000669565-Thymidylic acid,2TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS466.1357Semi standard non polar2701.7742
RI000669575-Thymidylic acid,2TMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O2)C(=O)N([Si](C)(C)C)C1=OTMS466.1357Semi standard non polar2639.9382
RI000669585-Thymidylic acid,2TMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS466.1357Semi standard non polar2756.2156
RI000669595-Thymidylic acid,2TMS,isomer#4JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS466.1357Semi standard non polar2744.133
RI000669605-Thymidylic acid,3TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS538.1752Semi standard non polar2752.8682
RI000669615-Thymidylic acid,3TMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS538.1752Semi standard non polar2722.3516
RI000669625-Thymidylic acid,3TMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS538.1752Semi standard non polar2755.687
RI000669635-Thymidylic acid,4TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS610.2147Semi standard non polar2774.233
RI000669645-Thymidylic acid,2TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS550.2296Semi standard non polar3183.52
RI000669655-Thymidylic acid,2TBDMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS550.2296Semi standard non polar3121.5718
RI000669665-Thymidylic acid,2TBDMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS550.2296Semi standard non polar3208.094
RI000669675-Thymidylic acid,2TBDMS,isomer#4JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS550.2296Semi standard non polar3198.8064
RI000669685-Thymidylic acid,3TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS664.316Semi standard non polar3407.3438
RI000669695-Thymidylic acid,3TBDMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Semi standard non polar3404.8438
RI000669705-Thymidylic acid,3TBDMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Semi standard non polar3428.4126
RI000669715-Thymidylic acid,4TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS778.4025Semi standard non polar3615.0723
RI000669725-Thymidylic acid,2TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS466.1357Standard polar3835.788
RI000669735-Thymidylic acid,2TMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O2)C(=O)N([Si](C)(C)C)C1=OTMS466.1357Standard polar4280.9404
RI000669745-Thymidylic acid,2TMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS466.1357Standard polar3546.0232
RI000669755-Thymidylic acid,2TMS,isomer#4JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS466.1357Standard polar3879.1504
Displaying retention index compounds 66951 - 66975 of 1722868 in total