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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14026 - 14050 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017101515-hydroxyindole thiazolidine carboxylate,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS566.2306Semi standard non polar2937.6138
RI017101505-hydroxyindole thiazolidine carboxylate,3TMS,isomer#4JsmolC[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C)=CN2[Si](C)(C)CTMS494.1911Semi standard non polar2916.7446
RI017101495-hydroxyindole thiazolidine carboxylate,3TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)CTMS494.1911Semi standard non polar2881.2793
RI017101485-hydroxyindole thiazolidine carboxylate,3TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS494.1911Semi standard non polar2908.48
RI017101475-hydroxyindole thiazolidine carboxylate,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1TMS494.1911Semi standard non polar2910.0781
RI017101465-hydroxyindole thiazolidine carboxylate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS734.4184Standard non polar3564.4602
RI017101455-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)CTBDMS620.3319Standard non polar3409.8828
RI017101445-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Standard non polar3432.7446
RI017101435-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1[Si](C)(C)C(C)(C)CTBDMS620.3319Standard non polar3450.6675
RI017101425-hydroxyindole thiazolidine carboxylate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C23)N1TBDMS620.3319Standard non polar3457.0522
RI017101415-hydroxyindole thiazolidine carboxylate,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS566.2306Standard non polar2801.6243
RI017101405-hydroxyindole thiazolidine carboxylate,3TMS,isomer#4JsmolC[Si](C)(C)OC1=CC=C2C(=C1)C(CC1SCC(C(=O)O)N1[Si](C)(C)C)=CN2[Si](C)(C)CTMS494.1911Standard non polar2774.2607
RI017101395-hydroxyindole thiazolidine carboxylate,3TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O)C=C23)N1[Si](C)(C)CTMS494.1911Standard non polar2797.7805
RI017101385-hydroxyindole thiazolidine carboxylate,3TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=C[NH]C3=CC=C(O[Si](C)(C)C)C=C23)N1[Si](C)(C)CTMS494.1911Standard non polar2784.7437
RI017101375-hydroxyindole thiazolidine carboxylate,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CSC(CC2=CN([Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C=C23)N1TMS494.1911Standard non polar2805.9658
RI017101365-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1(O[Si](C)(C)C(C)(C)C)C(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS771.4589Standard polar3289.3982
RI017101355-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N=C(O)N=C1N=C(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1(O[Si](C)(C)C(C)(C)C)C(=O)[O-]TBDMS657.3725Standard polar3424.204
RI017101345-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N=C(N=C1N=C(O)N([Si](C)(C)C(C)(C)C)C1(O[Si](C)(C)C(C)(C)C)C(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS657.3725Standard polar3317.177
RI017101335-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1(O)C(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS657.3725Standard polar3446.7092
RI017101325-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=N)N=C1N=C(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C1(O[Si](C)(C)C(C)(C)C)C(=O)[O-]TBDMS657.3725Standard polar3514.5754
RI017101315-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C(C)(C)C)NC1(O[Si](C)(C)C(C)(C)C)C(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS657.3725Standard polar4132.7124
RI017101305-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,5TMS,isomer#1JsmolC[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C)N([Si](C)(C)C)C1(O[Si](C)(C)C)C(=O)[O-])O[Si](C)(C)CTMS561.2242Standard polar3172.9368
RI017101295-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TMS,isomer#5JsmolC[Si](C)(C)N=C(O)N=C1N=C(O[Si](C)(C)C)N([Si](C)(C)C)C1(O[Si](C)(C)C)C(=O)[O-]TMS489.1846Standard polar3342.1396
RI017101285-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TMS,isomer#4JsmolC[Si](C)(C)N=C(N=C1N=C(O)N([Si](C)(C)C)C1(O[Si](C)(C)C)C(=O)[O-])O[Si](C)(C)CTMS489.1846Standard polar3192.7222
RI017101275-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H imidazole-5-carboxylate,4TMS,isomer#3JsmolC[Si](C)(C)N=C(N=C1N=C(O[Si](C)(C)C)N([Si](C)(C)C)C1(O)C(=O)[O-])O[Si](C)(C)CTMS489.1846Standard polar3405.6143
Displaying retention index compounds 14026 - 14050 of 1722868 in total