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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 15426 - 15450 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00015426Xanthine,2TMS,isomer#3JsmolC[Si](C)(C)N1C(=O)[NH]C2=C(C1=O)N([Si](C)(C)C)C=N2TMS296.1125Semi standard non polar1956.8691
RI00015427Xanthine,3TMS,isomer#1JsmolC[Si](C)(C)N1C(=O)C2=C(N=CN2[Si](C)(C)C)N([Si](C)(C)C)C1=OTMS368.152Semi standard non polar2067.7063
RI00015428Xanthine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C(=O)C2=C1N=C[NH]2TBDMS266.1199Semi standard non polar2096.2866
RI00015429Xanthine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)[NH]2TBDMS266.1199Semi standard non polar2159.6843
RI00015430Xanthine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C2=C([NH]C=N2)C1=OTBDMS266.1199Semi standard non polar2072.924
RI00015431Xanthine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)C2=C(N=C[NH]2)N([Si](C)(C)C(C)(C)C)C1=OTBDMS380.2064Semi standard non polar2285.6567
RI00015432Xanthine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)N2[Si](C)(C)C(C)(C)CTBDMS380.2064Semi standard non polar2327.4453
RI00015433Xanthine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C2=C(C1=O)N([Si](C)(C)C(C)(C)C)C=N2TBDMS380.2064Semi standard non polar2354.6687
RI00015434Xanthine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS494.2929Semi standard non polar2560.4666
RI00015435Xanthine,1TMS,isomer#1JsmolC[Si](C)(C)N1C(=O)[NH]C(=O)C2=C1N=C[NH]2TMS224.073Standard polar2884.1423
RI00015436Xanthine,1TMS,isomer#2JsmolC[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)[NH]2TMS224.073Standard polar2738.476
RI00015437Xanthine,1TMS,isomer#3JsmolC[Si](C)(C)N1C(=O)[NH]C2=C([NH]C=N2)C1=OTMS224.073Standard polar2926.7244
RI00015438Xanthine,2TMS,isomer#1JsmolC[Si](C)(C)N1C(=O)C2=C(N=C[NH]2)N([Si](C)(C)C)C1=OTMS296.1125Standard polar2493.3071
RI00015439Xanthine,2TMS,isomer#2JsmolC[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)N2[Si](C)(C)CTMS296.1125Standard polar2381.9163
RI00015440Xanthine,2TMS,isomer#3JsmolC[Si](C)(C)N1C(=O)[NH]C2=C(C1=O)N([Si](C)(C)C)C=N2TMS296.1125Standard polar2425.284
RI00015441Xanthine,3TMS,isomer#1JsmolC[Si](C)(C)N1C(=O)C2=C(N=CN2[Si](C)(C)C)N([Si](C)(C)C)C1=OTMS368.152Standard polar2199.751
RI00015442Xanthine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C(=O)C2=C1N=C[NH]2TBDMS266.1199Standard polar2853.101
RI00015443Xanthine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)[NH]2TBDMS266.1199Standard polar2780.427
RI00015444Xanthine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C2=C([NH]C=N2)C1=OTBDMS266.1199Standard polar2915.727
RI00015445Xanthine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)C2=C(N=C[NH]2)N([Si](C)(C)C(C)(C)C)C1=OTBDMS380.2064Standard polar2529.3748
RI00015446Xanthine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)[NH]C(=O)N2[Si](C)(C)C(C)(C)CTBDMS380.2064Standard polar2468.297
RI00015447Xanthine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C(=O)[NH]C2=C(C1=O)N([Si](C)(C)C(C)(C)C)C=N2TBDMS380.2064Standard polar2525.2085
RI00015448Xanthine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS494.2929Standard polar2481.2595
RI00015449Xanthosine 5-triphosphate,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O[C@@H](N2C=NC3=C(O)N=C(O)N=C32)[C@@H]1OTMS596.0142Semi standard non polar4309.4834
RI00015450Xanthosine 5-triphosphate,1TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O[C@H]1N1C=NC2=C(O)N=C(O)N=C21TMS596.0142Semi standard non polar4312.5967
Displaying retention index compounds 15426 - 15450 of 1722868 in total