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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14251 - 14275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017099265-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 non polar4704.8896
RI017099255-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 non polar4745.1475
RI017099245-formyl-tetrahydrofolate,2TBDMS,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)[NH]1)[Si](C)(C)C(C)(C)CTBDMS699.3243Standard non polar4736.487
RI017099235-formyl-tetrahydrofolate,1TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1NCC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTBDMS585.2378Standard non polar4492.844
RI017099225-formyl-tetrahydrofolate,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N)[NH]3)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TBDMS585.2378Standard non polar4372.3413
RI017099215-formyl-tetrahydrofolate,1TBDMS,isomer#3JsmolCC(C)(C)[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=C1TBDMS585.2378Standard non polar4362.5044
RI017099205-formyl-tetrahydrofolate,1TBDMS,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)=NC2=OTBDMS585.2378Standard non polar4433.5166
RI017099195-formyl-tetrahydrofolate,1TBDMS,isomer#1JsmolCC(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)[NH]1TBDMS585.2378Standard non polar4605.6636
RI017099185-formyl-tetrahydrofolate,5TMS,isomer#5JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)CTMS831.349Standard non polar4239.4697
RI017099175-formyl-tetrahydrofolate,5TMS,isomer#4JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS831.349Standard non polar4261.35
RI017099165-formyl-tetrahydrofolate,5TMS,isomer#3JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS831.349Standard non polar4225.3447
RI017099155-formyl-tetrahydrofolate,5TMS,isomer#2JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C2)N(C=O)C2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS831.349Standard non polar4362.3096
RI017099145-formyl-tetrahydrofolate,5TMS,isomer#1JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS831.349Standard non polar4333.922
RI017099135-formyl-tetrahydrofolate,4TMS,isomer#11JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS759.3095Standard non polar4174.8584
RI017099125-formyl-tetrahydrofolate,4TMS,isomer#10JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=OTMS759.3095Standard non polar4188.989
RI017099115-formyl-tetrahydrofolate,4TMS,isomer#9JsmolC[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=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)CTMS759.3095Standard non polar4171.9224
RI017099105-formyl-tetrahydrofolate,4TMS,isomer#8JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)CTMS759.3095Standard non polar4303.3813
RI017099095-formyl-tetrahydrofolate,4TMS,isomer#7JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)CTMS759.3095Standard non polar4276.002
RI017099085-formyl-tetrahydrofolate,4TMS,isomer#6JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS759.3095Standard non polar4208.689
RI017099075-formyl-tetrahydrofolate,4TMS,isomer#5JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C2)N(C=O)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS759.3095Standard non polar4299.341
RI017099065-formyl-tetrahydrofolate,4TMS,isomer#4JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS759.3095Standard non polar4284.014
RI017099055-formyl-tetrahydrofolate,4TMS,isomer#3JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS759.3095Standard non polar4299.4985
RI017099045-formyl-tetrahydrofolate,4TMS,isomer#2JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS759.3095Standard non polar4268.405
RI017099035-formyl-tetrahydrofolate,4TMS,isomer#1JsmolC[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(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS759.3095Standard non polar4393.795
RI017099025-formyl-tetrahydrofolate,3TMS,isomer#14JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS687.2699Standard non polar4111.768
Displaying retention index compounds 14251 - 14275 of 1722868 in total