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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14276 - 14300 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017099015-formyl-tetrahydrofolate,3TMS,isomer#13JsmolC[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)=NC2=OTMS687.2699Standard non polar4206.512
RI017099005-formyl-tetrahydrofolate,3TMS,isomer#12JsmolC[Si](C)(C)N(CC1CN([Si](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=C1TMS687.2699Standard non polar4139.962
RI017098995-formyl-tetrahydrofolate,3TMS,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)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS687.2699Standard non polar4219.12
RI017098985-formyl-tetrahydrofolate,3TMS,isomer#10JsmolC[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)[NH]1TMS687.2699Standard non polar4175.711
RI017098975-formyl-tetrahydrofolate,3TMS,isomer#9JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1)N2C=OTMS687.2699Standard non polar4267.2104
RI017098965-formyl-tetrahydrofolate,3TMS,isomer#8JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)[Si](C)(C)C)N2C=OTMS687.2699Standard non polar4248.9062
RI017098955-formyl-tetrahydrofolate,3TMS,isomer#7JsmolC[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=C3)N2C=O)N1[Si](C)(C)CTMS687.2699Standard non polar4286.6016
RI017098945-formyl-tetrahydrofolate,3TMS,isomer#6JsmolC[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)N2C=O)N1[Si](C)(C)CTMS687.2699Standard non polar4258.3154
RI017098935-formyl-tetrahydrofolate,3TMS,isomer#5JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)CTMS687.2699Standard non polar4378.7915
RI017098925-formyl-tetrahydrofolate,3TMS,isomer#4JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS687.2699Standard non polar4281.0283
RI017098915-formyl-tetrahydrofolate,3TMS,isomer#3JsmolC[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)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS687.2699Standard non polar4277.993
RI017098905-formyl-tetrahydrofolate,3TMS,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([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS687.2699Standard non polar4343.721
RI017098895-formyl-tetrahydrofolate,3TMS,isomer#1JsmolC[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)[Si](C)(C)CTMS687.2699Standard non polar4371.3647
RI017098885-formyl-tetrahydrofolate,2TMS,isomer#11JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS615.2304Standard non polar4179.482
RI017098875-formyl-tetrahydrofolate,2TMS,isomer#10JsmolC[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=C1TMS615.2304Standard non polar4107.488
RI017098865-formyl-tetrahydrofolate,2TMS,isomer#9JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS615.2304Standard non polar4182.705
RI017098855-formyl-tetrahydrofolate,2TMS,isomer#8JsmolC[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)=NC2=OTMS615.2304Standard non polar4273.4663
RI017098845-formyl-tetrahydrofolate,2TMS,isomer#7JsmolC[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)=NC2=OTMS615.2304Standard non polar4189.161
RI017098835-formyl-tetrahydrofolate,2TMS,isomer#6JsmolC[Si](C)(C)N(CC1CN([Si](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=C1TMS615.2304Standard non polar4193.0327
RI017098825-formyl-tetrahydrofolate,2TMS,isomer#5JsmolC[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=C3)N2C=O)[NH]1TMS615.2304Standard non polar4277.238
RI017098815-formyl-tetrahydrofolate,2TMS,isomer#4JsmolC[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)N2C=O)[NH]1TMS615.2304Standard non polar4282.33
RI017098805-formyl-tetrahydrofolate,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTMS615.2304Standard non polar4342.998
RI017098795-formyl-tetrahydrofolate,2TMS,isomer#2JsmolC[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)CTMS615.2304Standard non polar4375.119
RI017098785-formyl-tetrahydrofolate,2TMS,isomer#1JsmolC[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)CTMS615.2304Standard non polar4368.5283
RI017098775-formyl-tetrahydrofolate,1TMS,isomer#5JsmolC[Si](C)(C)N1C(N)=NC(=O)C2=C1NCC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTMS543.1909Standard non polar4298.4644
Displaying retention index compounds 14276 - 14300 of 1722868 in total