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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 10176 - 10200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01714001phenylacetohydroximoyl-cysteinylglycine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTBDMS422.157Semi standard non polar2909.342
RI01714000phenylacetohydroximoyl-cysteinylglycine,1TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTMS380.11Semi standard non polar2665.2993
RI01713999phenylacetohydroximoyl-cysteinylglycine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTBDMS422.157Standard non polar2716.9846
RI01713998phenylacetohydroximoyl-cysteinylglycine,1TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTMS380.11Standard non polar2493.2505
RI01713997p-coumaroyltyramine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS625.3803Standard polar3334.4585
RI01713996p-coumaroyltyramine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1TMS499.2394Standard polar3108.54
RI01713995p-coumaroyltyramine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS625.3803Semi standard non polar3851.5906
RI01713994p-coumaroyltyramine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1TMS499.2394Semi standard non polar3092.402
RI01713993p-coumaroyltyramine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS625.3803Standard non polar3439.9746
RI01713992p-coumaroyltyramine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1TMS499.2394Standard non polar2863.333
RI01713991p-coumaroyltriacetic acid lactone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TBDMS499.2342Standard polar3193.2817
RI01713990p-coumaroyltriacetic acid lactone,2TMS,isomer#1JsmolC[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TMS415.1403Standard polar3068.232
RI01713989p-coumaroyltriacetic acid lactone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TBDMS499.2342Semi standard non polar3499.82
RI01713988p-coumaroyltriacetic acid lactone,2TMS,isomer#1JsmolC[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TMS415.1403Semi standard non polar2969.4363
RI01713987p-coumaroyltriacetic acid lactone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TBDMS499.2342Standard non polar3282.737
RI01713986p-coumaroyltriacetic acid lactone,2TMS,isomer#1JsmolC[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C)C=C1)=CC1=CC([O-])=CC(=O)O1TMS415.1403Standard non polar2879.5842
RI01713985p-coumaroyltriacetate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)[O-])C=C(C=C(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS745.4177Standard polar3233.7341
RI01713984p-coumaroyltriacetate,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)[O-])C=C(C=C(C=CC1=CC=C(O)C=C1)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3327.0056
RI01713983p-coumaroyltriacetate,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3251.9404
RI01713982p-coumaroyltriacetate,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)[O-])CC(=CC(=O)C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3276.4846
RI01713981p-coumaroyltriacetate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)[O-])C=C(CC(=O)C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3249.9773
RI01713980p-coumaroyltriacetate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)=CC(=O)C=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3237.5464
RI01713979p-coumaroyltriacetate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)=CC(=O)CC(=CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3254.7031
RI01713978p-coumaroyltriacetate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)CC(=O)[O-])C=C(C=CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)O[Si](C)(C)C(C)(C)CTBDMS631.3312Standard polar3206.778
RI01713977p-coumaroyltriacetate,2TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)OC(=CC(=O)C=CC1=CC=C(O)C=C1)C=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS517.2447Standard polar3412.4558
Displaying retention index compounds 10176 - 10200 of 1722868 in total