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Displaying retention index compounds 3676 - 3700 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
7,11-Dioxolanost-8-en-3-yl acetate,2TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS642.45Semi standard non polar3346.1143
7,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTMS570.4104Semi standard non polar3588.4468
7,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS570.4104Semi standard non polar3514.0166
7,11-Dioxolanost-8-en-3-yl acetate,2TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS726.5439Standard non polar3768.2903
7,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTBDMS612.4574Standard non polar3596.3032
7,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS612.4574Standard non polar3602.9814
7,11-Dioxolanost-8-en-3-yl acetate,2TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS642.45Standard non polar3427.976
7,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTMS570.4104Standard non polar3406.0808
7,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS570.4104Standard non polar3411.3567
4-Oxoproline,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(=O)[O-])N([Si](C)(C)C(C)(C)C)C1TBDMS356.2083Standard polar1996.2002
4-Oxoproline,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CN([Si](C)(C)C(C)(C)C)C(C(=O)[O-])C1TBDMS356.2083Standard polar2024.8162
4-Oxoproline,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1CC(=O)CC1C(=O)[O-]TBDMS242.1218Standard polar2014.9087
4-Oxoproline,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(=O)[O-])NC1TBDMS242.1218Standard polar2264.7598
4-Oxoproline,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CNC(C(=O)[O-])C1TBDMS242.1218Standard polar2397.4543
4-Oxoproline,2TMS,isomer#2JsmolC[Si](C)(C)OC1=CC(C(=O)[O-])N([Si](C)(C)C)C1TMS272.1144Standard polar1738.973
4-Oxoproline,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CN([Si](C)(C)C)C(C(=O)[O-])C1TMS272.1144Standard polar1788.0778
4-Oxoproline,1TMS,isomer#3JsmolC[Si](C)(C)N1CC(=O)CC1C(=O)[O-]TMS200.0748Standard polar1829.1417
4-Oxoproline,1TMS,isomer#2JsmolC[Si](C)(C)OC1=CC(C(=O)[O-])NC1TMS200.0748Standard polar2138.9028
4-Oxoproline,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CNC(C(=O)[O-])C1TMS200.0748Standard polar2310.4707
4-Oxoproline,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(=O)[O-])N([Si](C)(C)C(C)(C)C)C1TBDMS356.2083Semi standard non polar1882.2705
4-Oxoproline,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CN([Si](C)(C)C(C)(C)C)C(C(=O)[O-])C1TBDMS356.2083Semi standard non polar1944.4957
4-Oxoproline,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1CC(=O)CC1C(=O)[O-]TBDMS242.1218Semi standard non polar1585.2301
4-Oxoproline,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(=O)[O-])NC1TBDMS242.1218Semi standard non polar1580.706
4-Oxoproline,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CNC(C(=O)[O-])C1TBDMS242.1218Semi standard non polar1688.526
4-Oxoproline,2TMS,isomer#2JsmolC[Si](C)(C)OC1=CC(C(=O)[O-])N([Si](C)(C)C)C1TMS272.1144Semi standard non polar1444.9956
Displaying retention index compounds 3676 - 3700 of 1722868 in total