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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14076 - 14100 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017101015-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TMS,isomer#1JsmolC[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C)NC1(O[Si](C)(C)C)C(=O)[O-])O[Si](C)(C)CTMS489.1846Standard non polar1980.3192
RI017101005-formyl-tetrahydrofolate,3TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C1TBDMS813.4108Standard polar5960.048
RI017100995-formyl-tetrahydrofolate,3TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C2)N(C=O)C2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS813.4108Standard polar5952.587
RI017100985-formyl-tetrahydrofolate,3TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C1TBDMS813.4108Standard polar5790.624
RI017100975-formyl-tetrahydrofolate,3TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TBDMS813.4108Standard polar5897.9355
RI017100965-formyl-tetrahydrofolate,3TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]1TBDMS813.4108Standard polar5909.8325
RI017100955-formyl-tetrahydrofolate,3TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C1)N2C=OTBDMS813.4108Standard polar5779.8657
RI017100945-formyl-tetrahydrofolate,3TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)[Si](C)(C)C(C)(C)C)N2C=OTBDMS813.4108Standard polar5729.6377
RI017100935-formyl-tetrahydrofolate,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)CTBDMS813.4108Standard polar5912.5903
RI017100925-formyl-tetrahydrofolate,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)[Si](C)(C)C(C)(C)C)N2C=O)N1[Si](C)(C)C(C)(C)CTBDMS813.4108Standard polar5855.96
RI017100915-formyl-tetrahydrofolate,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)C(C)(C)CTBDMS813.4108Standard polar5706.8315
RI017100905-formyl-tetrahydrofolate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TBDMS813.4108Standard polar5802.8784
RI017100895-formyl-tetrahydrofolate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TBDMS813.4108Standard polar5745.8013
RI017100885-formyl-tetrahydrofolate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C2)N(C=O)C2=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS813.4108Standard polar5672.0044
RI017100875-formyl-tetrahydrofolate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS813.4108Standard polar5812.2017
RI017100865-formyl-tetrahydrofolate,2TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TBDMS699.3243Standard polar6362.3564
RI017100855-formyl-tetrahydrofolate,2TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C1TBDMS699.3243Standard polar6177.681
RI017100845-formyl-tetrahydrofolate,2TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TBDMS699.3243Standard polar6310.4414
RI017100835-formyl-tetrahydrofolate,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C2)N(C=O)C2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS699.3243Standard polar6276.8955
RI017100825-formyl-tetrahydrofolate,2TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C2)N(C=O)C2=C1[NH]C(N)=NC2=OTBDMS699.3243Standard polar6175.421
RI017100815-formyl-tetrahydrofolate,2TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TBDMS699.3243Standard polar6130.6865
RI017100805-formyl-tetrahydrofolate,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]1TBDMS699.3243Standard polar6384.0127
RI017100795-formyl-tetrahydrofolate,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]1TBDMS699.3243Standard polar6342.6816
RI017100785-formyl-tetrahydrofolate,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTBDMS699.3243Standard polar6172.7666
RI017100775-formyl-tetrahydrofolate,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)C(C)(C)CTBDMS699.3243Standard polar6317.6646
Displaying retention index compounds 14076 - 14100 of 1722868 in total