Displaying retention index compounds 1451 - 1475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Dihydroxyphenylacetic acid sulfate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CC(=O)OS(=O)(=O)O)C(O)=C1TBDMS362.0856Standard non polar2504.7217
Dihydroxyphenylacetic acid sulfate,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CC(=O)OS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1TMS464.1177Standard non polar2449.4326
Dihydroxyphenylacetic acid sulfate,2TMS,isomer#3JsmolC[Si](C)(C)OC1=CC(O)=CC=C1CC(=O)OS(=O)(=O)O[Si](C)(C)CTMS392.0781Standard non polar2334.7686
Dihydroxyphenylacetic acid sulfate,2TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(CC(=O)OS(=O)(=O)O[Si](C)(C)C)C(O)=C1TMS392.0781Standard non polar2337.3987
Dihydroxyphenylacetic acid sulfate,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CC(=O)OS(=O)(=O)O)C(O[Si](C)(C)C)=C1TMS392.0781Standard non polar2359.9988
Dihydroxyphenylacetic acid sulfate,1TMS,isomer#3JsmolC[Si](C)(C)OS(=O)(=O)OC(=O)CC1=CC=C(O)C=C1OTMS320.0386Standard non polar2211.7327
Dihydroxyphenylacetic acid sulfate,1TMS,isomer#2JsmolC[Si](C)(C)OC1=CC(O)=CC=C1CC(=O)OS(=O)(=O)OTMS320.0386Standard non polar2221.9414
Dihydroxyphenylacetic acid sulfate,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CC(=O)OS(=O)(=O)O)C(O)=C1TMS320.0386Standard non polar2220.1938
Caffeic acid sulfate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TBDMS372.071Standard polar3159.5889
Caffeic acid sulfate,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TMS330.024Standard polar3132.197
Caffeic acid sulfate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TBDMS372.071Semi standard non polar2505.3357
Caffeic acid sulfate,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TMS330.024Semi standard non polar2242.4932
Caffeic acid sulfate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TBDMS372.071Standard non polar2528.8135
Caffeic acid sulfate,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)/C=C/C1=CC=C([O-])C(OS(=O)(=O)[O-])=C1TMS330.024Standard non polar2271.267
Flortaucipir F18,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TBDMS376.1749Standard polar3229.552
Flortaucipir F18,1TMS,isomer#1JsmolC[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TMS334.1279Standard polar3156.3367
Flortaucipir F18,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TBDMS376.1749Semi standard non polar3093.884
Flortaucipir F18,1TMS,isomer#1JsmolC[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TMS334.1279Semi standard non polar2915.9377
Flortaucipir F18,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TBDMS376.1749Standard non polar2941.935
Flortaucipir F18,1TMS,isomer#1JsmolC[Si](C)(C)N1C2=CC=NC=C2C2=CC=C(C3=CC=C([18F])N=C3)C=C21TMS334.1279Standard non polar2716.63
Trilaciclib,2TBDMS,isomer#1JsmolCN1CCN(C2=CC=C(N(C3=NC=C4C=C5C(=O)N([Si](C)(C)C(C)(C)C)CC6(CCCCC6)N5C4=N3)[Si](C)(C)C(C)(C)C)N=C2)CC1TBDMS674.4272Standard polar5362.6816
Trilaciclib,1TBDMS,isomer#2JsmolCN1CCN(C2=CC=C(NC3=NC=C4C=C5C(=O)N([Si](C)(C)C(C)(C)C)CC6(CCCCC6)N5C4=N3)N=C2)CC1TBDMS560.3407Standard polar5719.2603
Trilaciclib,1TBDMS,isomer#1JsmolCN1CCN(C2=CC=C(N(C3=NC=C4C=C5C(=O)NCC6(CCCCC6)N5C4=N3)[Si](C)(C)C(C)(C)C)N=C2)CC1TBDMS560.3407Standard polar5714.1562
Trilaciclib,2TMS,isomer#1JsmolCN1CCN(C2=CC=C(N(C3=NC=C4C=C5C(=O)N([Si](C)(C)C)CC6(CCCCC6)N5C4=N3)[Si](C)(C)C)N=C2)CC1TMS590.3333Standard polar5240.3306
Trilaciclib,1TMS,isomer#2JsmolCN1CCN(C2=CC=C(NC3=NC=C4C=C5C(=O)N([Si](C)(C)C)CC6(CCCCC6)N5C4=N3)N=C2)CC1TMS518.2938Standard polar5571.2334
Displaying retention index compounds 1451 - 1475 of 1722868 in total