Displaying retention index compounds 351 - 375 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Iodotyrosine,3TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CC1=CC=C(O[Si](C)(C)C)C(I)=C1)C(=O)O[Si](C)(C)CTMS523.0891Standard polar2140.292
Iodotyrosine,3TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1ITMS523.0891Standard polar2284.673
Iodotyrosine,3TMS,isomer#3JsmolC[Si](C)(C)OC(=O)[C@H](CC1=CC=C(O)C(I)=C1)N([Si](C)(C)C)[Si](C)(C)CTMS523.0891Standard polar2304.3867
Iodotyrosine,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C(I)=C1)N([Si](C)(C)C)[Si](C)(C)CTMS595.1286Standard polar2095.634
Iodotyrosine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N[C@@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C(I)=C1)C(=O)O[Si](C)(C)C(C)(C)CTBDMS649.23Standard polar2530.2478
Iodotyrosine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1ITBDMS649.23Standard polar2588.3015
Iodotyrosine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC=C(O)C(I)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS649.23Standard polar2596.5298
Iodotyrosine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C(I)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS763.3164Standard polar2545.6096
3-Methoxytyramine,1TMS,isomer#1JsmolCOC1=CC(CCN)=CC=C1O[Si](C)(C)CTMS239.1342Semi standard non polar1618.5693
3-Methoxytyramine,1TMS,isomer#2JsmolCOC1=CC(CCN[Si](C)(C)C)=CC=C1OTMS239.1342Semi standard non polar1721.3655
3-Methoxytyramine,1TBDMS,isomer#1JsmolCOC1=CC(CCN)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS281.1811Semi standard non polar1883.4069
3-Methoxytyramine,1TBDMS,isomer#2JsmolCOC1=CC(CCN[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS281.1811Semi standard non polar1992.0576
3-MethoxytyramineJsmolCOC1=C(O)C=CC(CCN)=C1Underivatized167.0946Standard polar2467.0303
3-Methoxytyramine,2TMS,isomer#1JsmolCOC1=CC(CCN[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS311.1737Standard non polar1846.1597
3-Methoxytyramine,2TMS,isomer#2JsmolCOC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1OTMS311.1737Standard non polar2026.3635
3-Methoxytyramine,3TMS,isomer#1JsmolCOC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS383.2132Standard non polar2003.6721
3-Methoxytyramine,2TBDMS,isomer#1JsmolCOC1=CC(CCN[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS395.2676Standard non polar2294.7334
3-Methoxytyramine,2TBDMS,isomer#2JsmolCOC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS395.2676Standard non polar2431.006
3-Methoxytyramine,3TBDMS,isomer#1JsmolCOC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS509.3541Standard non polar2600.121
3-MethoxytyramineJsmolCOC1=C(O)C=CC(CCN)=C1Underivatized167.0946Standard non polar1657.5372
3-MethoxytyramineJsmolCOC1=C(O)C=CC(CCN)=C1Underivatized167.0946Semi standard non polar1568.372
3-Methoxytyramine,2TMS,isomer#1JsmolCOC1=CC(CCN[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS311.1737Semi standard non polar1770.6837
3-Methoxytyramine,2TMS,isomer#2JsmolCOC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1OTMS311.1737Semi standard non polar1938.6321
3-Methoxytyramine,3TMS,isomer#1JsmolCOC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS383.2132Semi standard non polar1998.623
3-Methoxytyramine,2TBDMS,isomer#1JsmolCOC1=CC(CCN[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS395.2676Semi standard non polar2258.3945
Displaying retention index compounds 351 - 375 of 1722868 in total