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Displaying retention index compounds 66976 - 67000 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
5-Thymidylic acid,3TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=OTMS538.1752Standard polar3335.6306
5-Thymidylic acid,3TMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS538.1752Standard polar3579.0686
5-Thymidylic acid,3TMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS538.1752Standard polar3345.003
5-Thymidylic acid,4TMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=OTMS610.2147Standard polar3165.0706
5-Thymidylic acid,2TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS550.2296Standard polar3929.3928
5-Thymidylic acid,2TBDMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS550.2296Standard polar4200.4004
5-Thymidylic acid,2TBDMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS550.2296Standard polar3725.7368
5-Thymidylic acid,2TBDMS,isomer#4JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS550.2296Standard polar3916.9263
5-Thymidylic acid,3TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=OTBDMS664.316Standard polar3595.1157
5-Thymidylic acid,3TBDMS,isomer#2JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Standard polar3708.0776
5-Thymidylic acid,3TBDMS,isomer#3JsmolCC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS664.316Standard polar3567.9175
5-Thymidylic acid,4TBDMS,isomer#1JsmolCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS778.4025Standard polar3460.634
L-Glutamic acid 5-phosphate,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H](N)CCC(=O)OP(=O)(O)OTMS299.059Semi standard non polar1925.7639
L-Glutamic acid 5-phosphate,1TMS,isomer#2JsmolC[Si](C)(C)OP(=O)(O)OC(=O)CC[C@H](N)C(=O)OTMS299.059Semi standard non polar2010.5321
L-Glutamic acid 5-phosphate,1TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CCC(=O)OP(=O)(O)O)C(=O)OTMS299.059Semi standard non polar2035.7627
L-Glutamic acid 5-phosphate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=O)OP(=O)(O)OTBDMS341.106Semi standard non polar2193.4712
L-Glutamic acid 5-phosphate,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OP(=O)(O)OC(=O)CC[C@H](N)C(=O)OTBDMS341.106Semi standard non polar2259.0708
L-Glutamic acid 5-phosphate,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)OP(=O)(O)O)C(=O)OTBDMS341.106Semi standard non polar2282.725
L-Glutamic acid 5-phosphateJsmolN[C@@H](CCC(=O)OP(O)(O)=O)C(O)=OUnderivatized227.0195Standard polar2772.375
L-Glutamic acid 5-phosphateJsmolN[C@@H](CCC(=O)OP(O)(O)=O)C(O)=OUnderivatized227.0195Standard non polar1571.2635
L-Glutamic acid 5-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H](N)CCC(=O)OP(=O)(O)O[Si](C)(C)CTMS371.0985Standard non polar2005.43
L-Glutamic acid 5-phosphate,2TMS,isomer#2JsmolC[Si](C)(C)N[C@@H](CCC(=O)OP(=O)(O)O)C(=O)O[Si](C)(C)CTMS371.0985Standard non polar2053.6177
L-Glutamic acid 5-phosphate,2TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(OC(=O)CC[C@H](N)C(=O)O)O[Si](C)(C)CTMS371.0985Standard non polar2002.8827
L-Glutamic acid 5-phosphate,2TMS,isomer#4JsmolC[Si](C)(C)N[C@@H](CCC(=O)OP(=O)(O)O[Si](C)(C)C)C(=O)OTMS371.0985Standard non polar2037.82
L-Glutamic acid 5-phosphate,2TMS,isomer#5JsmolC[Si](C)(C)N([C@@H](CCC(=O)OP(=O)(O)O)C(=O)O)[Si](C)(C)CTMS371.0985Standard non polar2117.862
Displaying retention index compounds 66976 - 67000 of 1722868 in total