Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 15376 - 15400 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00015376Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#29JsmolCC(=O)N([C@H]1[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)CTBDMS835.2545Semi standard non polar4625.118
RI00015377Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#30JsmolCC(=O)N[C@H]1[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1OTBDMS835.2545Semi standard non polar4731.1665
RI00015378Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#31JsmolCC(=O)N[C@H]1[C@@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1OTBDMS835.2545Semi standard non polar4729.182
RI00015379Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#32JsmolCC(=O)N([C@H]1[C@@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)CTBDMS835.2545Semi standard non polar4660.1543
RI00015380Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#33JsmolCC(=O)N[C@H]1[C@@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1OTBDMS835.2545Semi standard non polar4787.16
RI00015381Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#34JsmolCC(=O)N([C@H]1[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)CTBDMS835.2545Semi standard non polar4661.276
RI00015382Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#35JsmolCC(=O)N[C@H]1[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1OTBDMS835.2545Semi standard non polar4775.464
RI00015383Uridine diphosphate-N-acetylglucosamine,2TBDMS,isomer#36JsmolCC(=O)N([C@H]1[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)CTBDMS835.2545Semi standard non polar4746.654
RI00015384Uridine diphosphate-N-acetylglucosamineJsmolCC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized607.0816Standard polar5123.992
RI00015385Uridine diphosphate-N-acetylglucosamineJsmolCC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized607.0816Standard non polar3392.9404
RI00015386Uridine diphosphate-N-acetylglucosamineJsmolCC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized607.0816Semi standard non polar5095.725
RI00015387Vanillylmandelic acid,1TMS,isomer#1JsmolCOC1=CC([C@H](O)C(=O)O)=CC=C1O[Si](C)(C)CTMS270.0924Semi standard non polar1884.9817
RI00015388Vanillylmandelic acid,1TMS,isomer#2JsmolCOC1=CC([C@H](O[Si](C)(C)C)C(=O)O)=CC=C1OTMS270.0924Semi standard non polar1852.4832
RI00015389Vanillylmandelic acid,1TMS,isomer#3JsmolCOC1=CC([C@H](O)C(=O)O[Si](C)(C)C)=CC=C1OTMS270.0924Semi standard non polar1814.7222
RI00015390Vanillylmandelic acid,2TMS,isomer#1JsmolCOC1=CC([C@H](O[Si](C)(C)C)C(=O)O)=CC=C1O[Si](C)(C)CTMS342.1319Semi standard non polar1884.7811
RI00015391Vanillylmandelic acid,2TMS,isomer#2JsmolCOC1=CC([C@H](O)C(=O)O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS342.1319Semi standard non polar1880.9402
RI00015392Vanillylmandelic acid,2TMS,isomer#3JsmolCOC1=CC([C@H](O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC=C1OTMS342.1319Semi standard non polar1897.1937
RI00015393Vanillylmandelic acid,3TMS,isomer#1JsmolCOC1=CC([C@H](O[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS414.1714Semi standard non polar1912.7716
RI00015394Vanillylmandelic acid,1TBDMS,isomer#1JsmolCOC1=CC([C@H](O)C(=O)O)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS312.1393Semi standard non polar2170.0422
RI00015395Vanillylmandelic acid,1TBDMS,isomer#2JsmolCOC1=CC([C@H](O[Si](C)(C)C(C)(C)C)C(=O)O)=CC=C1OTBDMS312.1393Semi standard non polar2137.9731
RI00015396Vanillylmandelic acid,1TBDMS,isomer#3JsmolCOC1=CC([C@H](O)C(=O)O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS312.1393Semi standard non polar2073.0647
RI00015397Vanillylmandelic acid,2TBDMS,isomer#1JsmolCOC1=CC([C@H](O[Si](C)(C)C(C)(C)C)C(=O)O)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS426.2258Semi standard non polar2416.3364
RI00015398Vanillylmandelic acid,2TBDMS,isomer#2JsmolCOC1=CC([C@H](O)C(=O)O[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS426.2258Semi standard non polar2358.9712
RI00015399Vanillylmandelic acid,2TBDMS,isomer#3JsmolCOC1=CC([C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS426.2258Semi standard non polar2371.1123
RI00015400Vanillylmandelic acid,3TBDMS,isomer#1JsmolCOC1=CC([C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS540.3123Semi standard non polar2582.2205
Displaying retention index compounds 15376 - 15400 of 1722868 in total