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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 13201 - 13225 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017109767,8-dihydromonapterin,5TMS,isomer#10JsmolC[Si](C)(C)N=C1N=C(O)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)CTMS615.2944Semi standard non polar2506.7969
RI017109757,8-dihydromonapterin,5TMS,isomer#9JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@@H](O)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 polar2524.4473
RI017109747,8-dihydromonapterin,5TMS,isomer#8JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC([C@H](O)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2TMS615.2944Semi standard non polar2475.8647
RI017109737,8-dihydromonapterin,5TMS,isomer#7JsmolC[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC([C@H](O)[C@H](CO[Si](C)(C)C)O[Si](C)(C)C)=N2)N1[Si](C)(C)CTMS615.2944Semi standard non polar2522.3748
RI017109727,8-dihydromonapterin,5TMS,isomer#6JsmolC[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=C2OTMS615.2944Semi standard non polar2514.1143
RI017109717,8-dihydromonapterin,5TMS,isomer#5JsmolC[Si](C)(C)N=C1N=C(O)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)=N2TMS615.2944Semi standard non polar2465.018
RI017109707,8-dihydromonapterin,5TMS,isomer#4JsmolC[Si](C)(C)N=C1N=C(O)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)CTMS615.2944Semi standard non polar2512.7288
RI017109697,8-dihydromonapterin,5TMS,isomer#3JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C1=NC2=C([NH]C(=N)N=C2O[Si](C)(C)C)N([Si](C)(C)C)C1TMS615.2944Semi standard non polar2508.181
RI017109687,8-dihydromonapterin,5TMS,isomer#2JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C)C(=N)N=C2O[Si](C)(C)CTMS615.2944Semi standard non polar2563.0981
RI017109677,8-dihydromonapterin,5TMS,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)[NH]1TMS615.2944Semi standard non polar2518.6782
RI017109667,8-dihydromonapterin,5TBDMS,isomer#21JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CO)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3521.2383
RI017109657,8-dihydromonapterin,5TBDMS,isomer#20JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O)[C@@H](O)CO[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3547.969
RI017109647,8-dihydromonapterin,5TBDMS,isomer#19JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CO[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3594.3765
RI017109637,8-dihydromonapterin,5TBDMS,isomer#18JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[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=C2O[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3560.8667
RI017109627,8-dihydromonapterin,5TBDMS,isomer#17JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)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](O)CO[Si](C)(C)C(C)(C)C)=N2TBDMS825.5291Standard non polar3634.4055
RI017109617,8-dihydromonapterin,5TBDMS,isomer#16JsmolCC(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](O)CO[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3477.4768
RI017109607,8-dihydromonapterin,5TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O)[C@H](CO)O[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3531.3203
RI017109597,8-dihydromonapterin,5TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O[Si](C)(C)C(C)(C)C)[C@H](CO)O[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3589.633
RI017109587,8-dihydromonapterin,5TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C(C)(C)C)C2=C1N=C([C@H](O[Si](C)(C)C(C)(C)C)[C@H](CO)O[Si](C)(C)C(C)(C)C)CN2[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3545.3137
RI017109577,8-dihydromonapterin,5TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)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)O[Si](C)(C)C(C)(C)C)=N2TBDMS825.5291Standard non polar3617.3518
RI017109567,8-dihydromonapterin,5TBDMS,isomer#11JsmolCC(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)O[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3456.5654
RI017109557,8-dihydromonapterin,5TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC([C@H](O)[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)CTBDMS825.5291Standard non polar3622.3074
RI017109547,8-dihydromonapterin,5TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(=N)N=C2O[Si](C)(C)C(C)(C)CTBDMS825.5291Standard non polar3582.6848
RI017109537,8-dihydromonapterin,5TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC([C@H](O)[C@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=N2TBDMS825.5291Standard non polar3661.493
RI017109527,8-dihydromonapterin,5TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC([C@H](O)[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)CTBDMS825.5291Standard non polar3484.7222
Displaying retention index compounds 13201 - 13225 of 1722868 in total