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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14226 - 14250 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017099515-formyl-tetrahydrofolate,1TMS,isomer#3JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS543.1909Semi standard non polar4507.809
RI017099505-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=OTMS543.1909Semi standard non polar4441.7793
RI017099495-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]1TMS543.1909Semi standard non polar4744.831
RI017099485-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 non polar4628.1816
RI017099475-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 non polar4745.3926
RI017099465-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 non polar4651.073
RI017099455-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 non polar4711.087
RI017099445-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 non polar4717.688
RI017099435-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 non polar4820.074
RI017099425-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 non polar4761.5312
RI017099415-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 non polar4838.6484
RI017099405-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 non polar4772.284
RI017099395-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 non polar4908.2715
RI017099385-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 non polar4839.664
RI017099375-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 non polar4795.095
RI017099365-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 non polar4874.985
RI017099355-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 non polar4905.5225
RI017099345-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 non polar4565.5024
RI017099335-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 non polar4487.2227
RI017099325-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 non polar4537.145
RI017099315-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 non polar4643.788
RI017099305-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 non polar4570.893
RI017099295-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 non polar4532.7744
RI017099285-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 non polar4673.9556
RI017099275-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 non polar4646.966
Displaying retention index compounds 14226 - 14250 of 1722868 in total