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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20426 - 20450 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703751(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C)CC(=O)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS493.2811Standard non polar2813.5981
RI01703750(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#1JsmolCCCCCC(=O)/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)CTMS493.2811Standard non polar2748.6807
RI01703749(3Z)-phytochromobilin,2TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS810.4219Standard polar6599.206
RI01703748(3Z)-phytochromobilin,2TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS810.4219Standard polar6196.4785
RI01703747(3Z)-phytochromobilin,2TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS810.4219Standard polar6537.8384
RI01703746(3Z)-phytochromobilin,1TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS696.3354Standard polar6925.302
RI01703745(3Z)-phytochromobilin,1TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS696.3354Standard polar7196.133
RI01703744(3Z)-phytochromobilin,1TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTBDMS696.3354Standard polar6841.659
RI01703743(3Z)-phytochromobilin,3TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS798.3675Standard polar6051.781
RI01703742(3Z)-phytochromobilin,2TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS726.328Standard polar6748.3535
RI01703741(3Z)-phytochromobilin,2TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS726.328Standard polar6332.166
RI01703740(3Z)-phytochromobilin,2TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS726.328Standard polar6661.1333
RI01703739(3Z)-phytochromobilin,1TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS654.2885Standard polar7010.5723
RI01703738(3Z)-phytochromobilin,1TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS654.2885Standard polar7263.43
RI01703737(3Z)-phytochromobilin,1TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTMS654.2885Standard polar6909.9985
RI01703736(3Z)-phytochromobilin,2TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS810.4219Semi standard non polar5209.834
RI01703735(3Z)-phytochromobilin,2TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS810.4219Semi standard non polar5037.035
RI01703734(3Z)-phytochromobilin,2TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS810.4219Semi standard non polar5275.9297
RI01703733(3Z)-phytochromobilin,1TBDMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C(C)(C)C)C1=OTBDMS696.3354Semi standard non polar5116.1763
RI01703732(3Z)-phytochromobilin,1TBDMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C(C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTBDMS696.3354Semi standard non polar5260.188
RI01703731(3Z)-phytochromobilin,1TBDMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C(C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)NC1=OTBDMS696.3354Semi standard non polar5161.6704
RI01703730(3Z)-phytochromobilin,3TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS798.3675Semi standard non polar4717.395
RI01703729(3Z)-phytochromobilin,2TMS,isomer#3JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4NC(=O)C(C)C4=CC)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS726.328Semi standard non polar4921.818
RI01703728(3Z)-phytochromobilin,2TMS,isomer#2JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)[NH]3)C(CCC(=O)[O-])=C2C)N([Si](C)(C)C)C1=OTMS726.328Semi standard non polar4687.0186
RI01703727(3Z)-phytochromobilin,2TMS,isomer#1JsmolC=CC1=C(C)C(=CC2=NC(=CC3=C(CCC(=O)[O-])C(C)=C(C=C4C(=CC)C(C)C(=O)N4[Si](C)(C)C)N3[Si](C)(C)C)C(CCC(=O)[O-])=C2C)NC1=OTMS726.328Semi standard non polar5008.1143
Displaying retention index compounds 20426 - 20450 of 1722868 in total