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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 9751 - 9775 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01714426salutaridinol,2TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS557.3357Semi standard non polar3133.556
RI01714425salutaridinol,1TBDMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS443.2492Semi standard non polar2948.7861
RI01714424salutaridinol,1TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1OTBDMS443.2492Semi standard non polar2986.1836
RI01714423salutaridinol,2TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1O[Si](C)(C)CTMS473.2418Semi standard non polar2713.0312
RI01714422salutaridinol,1TMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)CTMS401.2022Semi standard non polar2720.5469
RI01714421salutaridinol,1TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1OTMS401.2022Semi standard non polar2732.2932
RI01714420salutaridinol,2TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS557.3357Standard non polar3175.5854
RI01714419salutaridinol,1TBDMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS443.2492Standard non polar2917.6455
RI01714418salutaridinol,1TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1OTBDMS443.2492Standard non polar2896.218
RI01714417salutaridinol,2TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1O[Si](C)(C)CTMS473.2418Standard non polar2704.0325
RI01714416salutaridinol,1TMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)CTMS401.2022Standard non polar2657.1682
RI01714415salutaridinol,1TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1OTMS401.2022Standard non polar2622.0452
RI01714414salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C(C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)C(C)(C)CTBDMS604.3436Standard polar2889.6423
RI01714413salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)CTMS478.2027Standard polar2656.0571
RI01714412salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C(C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)C(C)(C)CTBDMS604.3436Semi standard non polar2959.287
RI01714411salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)CTMS478.2027Semi standard non polar2297.7456
RI01714410salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C(C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)C(C)(C)CTBDMS604.3436Standard non polar2697.6348
RI01714409salicyl-6-hydroxy-2-cyclohexene-on-oyl,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CCC=CC1(O[Si](C)(C)C)C(=O)OCC1=CC=CC=C1O[Si](C)(C)CTMS478.2027Standard non polar2219.0967
RI01714408S-sulfanylglutathione,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)SSCC(C(=O)N(CC(=O)[O-])[Si](C)(C)C(C)(C)C)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS677.2846Standard polar3872.5828
RI01714407S-sulfanylglutathione,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSS)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS563.1981Standard polar4093.3918
RI01714406S-sulfanylglutathione,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)SSCC(NC(=O)CCC([N+])C(=O)[O-])C(=O)N(CC(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS563.1981Standard polar4042.6614
RI01714405S-sulfanylglutathione,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)SSCC(C(=O)NCC(=O)[O-])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS563.1981Standard polar4055.977
RI01714404S-sulfanylglutathione,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSS)NC(=O)CCC([N+])C(=O)[O-]TBDMS449.1116Standard polar4419.159
RI01714403S-sulfanylglutathione,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSS)C(=O)NCC(=O)[O-]TBDMS449.1116Standard polar4420.5303
RI01714402S-sulfanylglutathione,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)SSCC(NC(=O)CCC([N+])C(=O)[O-])C(=O)NCC(=O)[O-]TBDMS449.1116Standard polar4452.469
Displaying retention index compounds 9751 - 9775 of 1722868 in total