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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 13176 - 13200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017110017,8-dihydromonapterin,5TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(=N)N=C2OTBDMS825.5291Semi standard non polar3503.848
RI017110007,8-dihydromonapterin,5TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC([C@H](O[Si](C)(C)C(C)(C)C)[C@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=N2TBDMS825.5291Semi standard non polar3426.1667
RI017109997,8-dihydromonapterin,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC([C@H](O[Si](C)(C)C(C)(C)C)[C@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Semi standard non polar3540.6853
RI017109987,8-dihydromonapterin,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(=N)N=C2O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1TBDMS825.5291Semi standard non polar3452.6428
RI017109977,8-dihydromonapterin,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(=N)N=C2O[Si](C)(C)C(C)(C)CTBDMS825.5291Semi standard non polar3522.1592
RI017109967,8-dihydromonapterin,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC([C@H](O[Si](C)(C)C(C)(C)C)[C@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=N2)[NH]1TBDMS825.5291Semi standard non polar3446.2957
RI017109957,8-dihydromonapterin,7TMS,isomer#1JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS759.3734Semi standard non polar2627.9856
RI017109947,8-dihydromonapterin,6TMS,isomer#7JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@@H](O)CO[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS687.3339Semi standard non polar2576.2197
RI017109937,8-dihydromonapterin,6TMS,isomer#6JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS687.3339Semi standard non polar2583.4268
RI017109927,8-dihydromonapterin,6TMS,isomer#5JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS687.3339Semi standard non polar2563.681
RI017109917,8-dihydromonapterin,6TMS,isomer#4JsmolC[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS687.3339Semi standard non polar2557.2673
RI017109907,8-dihydromonapterin,6TMS,isomer#3JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(=N)N=C2O[Si](C)(C)CTMS687.3339Semi standard non polar2586.8376
RI017109897,8-dihydromonapterin,6TMS,isomer#2JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2TMS687.3339Semi standard non polar2541.1313
RI017109887,8-dihydromonapterin,6TMS,isomer#1JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC([C@H](O[Si](C)(C)C)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS687.3339Semi standard non polar2566.687
RI017109877,8-dihydromonapterin,5TMS,isomer#21JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@@H](O)CO)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2542.4114
RI017109867,8-dihydromonapterin,5TMS,isomer#20JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O)[C@@H](O)CO[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2526.7866
RI017109857,8-dihydromonapterin,5TMS,isomer#19JsmolC[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@@H](O)CO[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2510.2983
RI017109847,8-dihydromonapterin,5TMS,isomer#18JsmolC[Si](C)(C)OC[C@H](O)[C@@H](O[Si](C)(C)C)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(=N)N=C2O[Si](C)(C)CTMS615.2944Semi standard non polar2539.1104
RI017109837,8-dihydromonapterin,5TMS,isomer#17JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@@H](O)CO[Si](C)(C)C)=N2TMS615.2944Semi standard non polar2489.6428
RI017109827,8-dihydromonapterin,5TMS,isomer#16JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC([C@H](O[Si](C)(C)C)[C@@H](O)CO[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2538.936
RI017109817,8-dihydromonapterin,5TMS,isomer#15JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC([C@H](O)[C@H](CO)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2521.8333
RI017109807,8-dihydromonapterin,5TMS,isomer#14JsmolC[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2518.8794
RI017109797,8-dihydromonapterin,5TMS,isomer#13JsmolC[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N=C([C@H](O[Si](C)(C)C)[C@H](CO)O[Si](C)(C)C)CN2[Si](C)(C)CTMS615.2944Semi standard non polar2543.4607
RI017109787,8-dihydromonapterin,5TMS,isomer#12JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC([C@H](O[Si](C)(C)C)[C@H](CO)O[Si](C)(C)C)=N2TMS615.2944Semi standard non polar2494.9119
RI017109777,8-dihydromonapterin,5TMS,isomer#11JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC([C@H](O[Si](C)(C)C)[C@H](CO)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2541.017
Displaying retention index compounds 13176 - 13200 of 1722868 in total