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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14151 - 14175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017100265-formyl-tetrahydrofolate,1TMS,isomer#2JsmolC[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)=NC2=OTMS543.1909Standard polar6692.3345
RI017100255-formyl-tetrahydrofolate,1TMS,isomer#1JsmolC[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)[NH]1TMS543.1909Standard polar7112.148
RI017100245-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=C1TBDMS813.4108Semi standard non polar4888.701
RI017100235-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=OTBDMS813.4108Semi standard non polar4835.0737
RI017100225-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=C1TBDMS813.4108Semi standard non polar4745.824
RI017100215-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=C1TBDMS813.4108Semi standard non polar4840.147
RI017100205-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]1TBDMS813.4108Semi standard non polar4951.5957
RI017100195-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=OTBDMS813.4108Semi standard non polar4865.213
RI017100185-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=OTBDMS813.4108Semi standard non polar4857.1006
RI017100175-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)CTBDMS813.4108Semi standard non polar5040.2695
RI017100165-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)CTBDMS813.4108Semi standard non polar4984.474
RI017100155-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)CTBDMS813.4108Semi standard non polar4924.92
RI017100145-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-]TBDMS813.4108Semi standard non polar4996.971
RI017100135-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=C1TBDMS813.4108Semi standard non polar4980.0522
RI017100125-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=OTBDMS813.4108Semi standard non polar4903.6865
RI017100115-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)CTBDMS813.4108Semi standard non polar5021.5854
RI017100105-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-]TBDMS699.3243Semi standard non polar4852.6216
RI017100095-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=C1TBDMS699.3243Semi standard non polar4802.4785
RI017100085-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=C1TBDMS699.3243Semi standard non polar4786.8145
RI017100075-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=OTBDMS699.3243Semi standard non polar4730.6406
RI017100065-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=OTBDMS699.3243Semi standard non polar4733.186
RI017100055-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=C1TBDMS699.3243Semi standard non polar4676.221
RI017100045-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]1TBDMS699.3243Semi standard non polar4965.95
RI017100035-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]1TBDMS699.3243Semi standard non polar4882.971
RI017100025-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=OTBDMS699.3243Semi standard non polar4820.6284
Displaying retention index compounds 14151 - 14175 of 1722868 in total