Displaying retention index compounds 126 - 150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
DeoxyuridineJsmolOC[C@H]1O[C@H](C[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized228.0746Standard non polar2205.1184
DeoxyuridineJsmolOC[C@H]1O[C@H](C[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized228.0746Semi standard non polar2386.8547
Deoxyuridine,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)CTMS444.1932Semi standard non polar2350.5208
Deoxyuridine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS570.3341Semi standard non polar3014.565
Deoxyuridine,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)CTMS444.1932Standard polar2627.7356
Deoxyuridine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS570.3341Standard polar2903.624
Deoxycytidine,1TMS,isomer#1JsmolC[Si](C)(C)O[C@H]1C[C@H](N2C=CC(N)=NC2=O)O[C@@H]1COTMS299.1301Semi standard non polar2307.797
Deoxycytidine,1TMS,isomer#2JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)C[C@@H]1OTMS299.1301Semi standard non polar2304.5786
Deoxycytidine,1TMS,isomer#3JsmolC[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO)O2)C=C1TMS299.1301Semi standard non polar2373.7026
Deoxycytidine,2TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)C[C@@H]1O[Si](C)(C)CTMS371.1697Semi standard non polar2266.8008
Deoxycytidine,2TMS,isomer#2JsmolC[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](CO)O2)C=C1TMS371.1697Semi standard non polar2356.2632
Deoxycytidine,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO[Si](C)(C)C)O2)C=C1TMS371.1697Semi standard non polar2348.1382
Deoxycytidine,2TMS,isomer#4JsmolC[Si](C)(C)N(C1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO)O2)C=C1)[Si](C)(C)CTMS371.1697Semi standard non polar2328.1748
Deoxycytidine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H](N2C=CC(N)=NC2=O)O[C@@H]1COTBDMS341.1771Semi standard non polar2565.2705
Deoxycytidine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)C[C@@H]1OTBDMS341.1771Semi standard non polar2558.6035
Deoxycytidine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO)O2)C=C1TBDMS341.1771Semi standard non polar2636.9604
Deoxycytidine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)C[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS455.2636Semi standard non polar2745.3853
Deoxycytidine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O2)C=C1TBDMS455.2636Semi standard non polar2813.4849
Deoxycytidine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)C=C1TBDMS455.2636Semi standard non polar2804.792
Deoxycytidine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)N([C@H]2C[C@H](O)[C@@H](CO)O2)C=C1)[Si](C)(C)C(C)(C)CTBDMS455.2636Semi standard non polar2776.3352
DeoxycytidineJsmolNC1=NC(=O)N(C=C1)[C@H]1C[C@H](O)[C@@H](CO)O1Underivatized227.0906Standard polar3645.4429
Deoxycytidine,3TMS,isomer#1JsmolC[Si](C)(C)NC1=NC(=O)N([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O2)C=C1TMS443.2092Standard non polar2462.3357
Deoxycytidine,3TMS,isomer#2JsmolC[Si](C)(C)O[C@H]1C[C@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)O[C@@H]1COTMS443.2092Standard non polar2478.5955
Deoxycytidine,3TMS,isomer#3JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C[C@@H]1OTMS443.2092Standard non polar2511.2937
Deoxycytidine,4TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C[C@@H]1O[Si](C)(C)CTMS515.2487Standard non polar2511.0312
Displaying retention index compounds 126 - 150 of 1722868 in total