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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14201 - 14225 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017099765-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=C1TMS687.2699Semi standard non polar4075.2744
RI017099755-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=C1TMS687.2699Semi standard non polar4179.818
RI017099745-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]1TMS687.2699Semi standard non polar4345.336
RI017099735-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=OTMS687.2699Semi standard non polar4268.5117
RI017099725-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=OTMS687.2699Semi standard non polar4280.5044
RI017099715-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)CTMS687.2699Semi standard non polar4432.247
RI017099705-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)CTMS687.2699Semi standard non polar4434.6157
RI017099695-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)CTMS687.2699Semi standard non polar4377.7236
RI017099685-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-]TMS687.2699Semi standard non polar4372.0107
RI017099675-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=C1TMS687.2699Semi standard non polar4365.541
RI017099665-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=OTMS687.2699Semi standard non polar4315.1733
RI017099655-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)CTMS687.2699Semi standard non polar4473.4077
RI017099645-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-]TMS615.2304Semi standard non polar4366.7183
RI017099635-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=C1TMS615.2304Semi standard non polar4309.929
RI017099625-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=C1TMS615.2304Semi standard non polar4356.34
RI017099615-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=OTMS615.2304Semi standard non polar4295.082
RI017099605-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=OTMS615.2304Semi standard non polar4228.762
RI017099595-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=C1TMS615.2304Semi standard non polar4217.8047
RI017099585-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]1TMS615.2304Semi standard non polar4542.0586
RI017099575-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]1TMS615.2304Semi standard non polar4511.5586
RI017099565-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=OTMS615.2304Semi standard non polar4446.7627
RI017099555-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)CTMS615.2304Semi standard non polar4600.556
RI017099545-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)CTMS615.2304Semi standard non polar4541.9307
RI017099535-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=OTMS543.1909Semi standard non polar4588.377
RI017099525-formyl-tetrahydrofolate,1TMS,isomer#4JsmolC[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-]TMS543.1909Semi standard non polar4558.804
Displaying retention index compounds 14201 - 14225 of 1722868 in total