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 14001 - 14025 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017101765-beta-pregnan-3,20 dione,1TBDMS,isomer#2JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Standard non polar2854.6606
RI017101755-beta-pregnan-3,20 dione,1TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Standard non polar2980.0244
RI017101745-beta-pregnan-3,20 dione,2TMS,isomer#4JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Standard non polar2781.735
RI017101735-beta-pregnan-3,20 dione,2TMS,isomer#3JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Standard non polar2757.359
RI017101725-beta-pregnan-3,20 dione,2TMS,isomer#2JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Standard non polar2789.9578
RI017101715-beta-pregnan-3,20 dione,2TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Standard non polar2766.391
RI017101705-beta-pregnan-3,20 dione,1TMS,isomer#4JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard non polar2733.5063
RI017101695-beta-pregnan-3,20 dione,1TMS,isomer#3JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard non polar2674.8232
RI017101685-beta-pregnan-3,20 dione,1TMS,isomer#2JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard non polar2657.1262
RI017101675-beta-pregnan-3,20 dione,1TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard non polar2729.088
RI017101665-hydroxyindole thiazolidine carboxylate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS734.4184Standard polar3439.2275
RI017101655-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)CTBDMS620.3319Standard polar3619.0974
RI017101645-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Standard polar3528.416
RI017101635-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Standard polar3519.8457
RI017101625-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1TBDMS620.3319Standard polar3688.9788
RI017101615-hydroxyindole thiazolidine carboxylate,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS566.2306Standard polar3163.4028
RI017101605-hydroxyindole thiazolidine carboxylate,3TMS,isomer#4JsmolC[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C)=CN2[Si](C)(C)CTMS494.1911Standard polar3465.8323
RI017101595-hydroxyindole thiazolidine carboxylate,3TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)CTMS494.1911Standard polar3376.3328
RI017101585-hydroxyindole thiazolidine carboxylate,3TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS494.1911Standard polar3312.2905
RI017101575-hydroxyindole thiazolidine carboxylate,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1TMS494.1911Standard polar3634.9194
RI017101565-hydroxyindole thiazolidine carboxylate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS734.4184Semi standard non polar3778.2554
RI017101555-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)CTBDMS620.3319Semi standard non polar3604.1936
RI017101545-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Semi standard non polar3542.7107
RI017101535-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Semi standard non polar3600.126
RI017101525-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1TBDMS620.3319Semi standard non polar3550.3904
Displaying retention index compounds 14001 - 14025 of 1722868 in total