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Displaying retention index compounds 65651 - 65675 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
N'-Formylkynurenine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS464.2527Standard non polar2777.4736
N'-Formylkynurenine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1NC=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS578.3391Standard non polar3023.36
N'-Formylkynurenine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS578.3391Standard non polar2947.7263
N'-Formylkynurenine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C=O)C1=CC=CC=C1C(=O)CC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS578.3391Standard non polar3047.9722
N'-Formylkynurenine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS692.4256Standard non polar3214.3623
N'-FormylkynurenineJsmolNC(CC(=O)C1=CC=CC=C1NC=O)C(O)=OUnderivatized236.0797Semi standard non polar2472.564
N'-Formylkynurenine,2TMS,isomer#1JsmolC[Si](C)(C)NC(CC(=O)C1=CC=CC=C1NC=O)C(=O)O[Si](C)(C)CTMS380.1588Semi standard non polar2335.8662
N'-Formylkynurenine,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C(N)CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)CTMS380.1588Semi standard non polar2206.5576
N'-Formylkynurenine,2TMS,isomer#3JsmolC[Si](C)(C)N(C(CC(=O)C1=CC=CC=C1NC=O)C(=O)O)[Si](C)(C)CTMS380.1588Semi standard non polar2467.954
N'-Formylkynurenine,2TMS,isomer#4JsmolC[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C)C(=O)OTMS380.1588Semi standard non polar2243.9297
N'-Formylkynurenine,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1NC=O)N([Si](C)(C)C)[Si](C)(C)CTMS452.1983Semi standard non polar2489.8484
N'-Formylkynurenine,3TMS,isomer#2JsmolC[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS452.1983Semi standard non polar2236.9292
N'-Formylkynurenine,3TMS,isomer#3JsmolC[Si](C)(C)N(C=O)C1=CC=CC=C1C(=O)CC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS452.1983Semi standard non polar2393.1465
N'-Formylkynurenine,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS524.2378Semi standard non polar2440.859
N'-Formylkynurenine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC(CC(=O)C1=CC=CC=C1NC=O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS464.2527Semi standard non polar2833.26
N'-Formylkynurenine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C(N)CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)CTBDMS464.2527Semi standard non polar2670.1807
N'-Formylkynurenine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(CC(=O)C1=CC=CC=C1NC=O)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS464.2527Semi standard non polar2968.492
N'-Formylkynurenine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS464.2527Semi standard non polar2721.5974
N'-Formylkynurenine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1NC=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS578.3391Semi standard non polar3185.0168
N'-Formylkynurenine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS578.3391Semi standard non polar2877.9458
N'-Formylkynurenine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C=O)C1=CC=CC=C1C(=O)CC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS578.3391Semi standard non polar3071.441
N'-Formylkynurenine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS692.4256Semi standard non polar3302.075
N'-Formylkynurenine,2TMS,isomer#1JsmolC[Si](C)(C)NC(CC(=O)C1=CC=CC=C1NC=O)C(=O)O[Si](C)(C)CTMS380.1588Standard polar3070.1763
N'-Formylkynurenine,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C(N)CC(=O)C1=CC=CC=C1N(C=O)[Si](C)(C)CTMS380.1588Standard polar3034.0432
N'-Formylkynurenine,2TMS,isomer#3JsmolC[Si](C)(C)N(C(CC(=O)C1=CC=CC=C1NC=O)C(=O)O)[Si](C)(C)CTMS380.1588Standard polar3284.6328
Displaying retention index compounds 65651 - 65675 of 1722868 in total