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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 16151 - 16175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017080262-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#2JsmolCC1=NC=C(C[N+]2=C(C(C)O)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS610.1279Standard polar4544.301
RI017080252-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N[Si](C)(C)C)=N1TMS610.1279Standard polar4603.435
RI017080242-(alpha-hydroxyethyl)thiamine diphosphate,3TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C(C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS808.3082Semi standard non polar3922.0913
RI017080232-(alpha-hydroxyethyl)thiamine diphosphate,2TBDMS,isomer#2JsmolCC1=NC=C(C[N+]2=C(C(C)O)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS694.2218Semi standard non polar3784.1323
RI017080222-(alpha-hydroxyethyl)thiamine diphosphate,2TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C(C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N[Si](C)(C)C(C)(C)C)=N1TBDMS694.2218Semi standard non polar3782.5552
RI017080212-(alpha-hydroxyethyl)thiamine diphosphate,3TMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS682.1674Semi standard non polar3425.2417
RI017080202-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#2JsmolCC1=NC=C(C[N+]2=C(C(C)O)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS610.1279Semi standard non polar3438.2068
RI017080192-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N[Si](C)(C)C)=N1TMS610.1279Semi standard non polar3440.7751
RI017080182-(alpha-hydroxyethyl)thiamine diphosphate,3TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C(C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS808.3082Standard non polar3803.953
RI017080172-(alpha-hydroxyethyl)thiamine diphosphate,2TBDMS,isomer#2JsmolCC1=NC=C(C[N+]2=C(C(C)O)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS694.2218Standard non polar3760.5898
RI017080162-(alpha-hydroxyethyl)thiamine diphosphate,2TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C(C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N[Si](C)(C)C(C)(C)C)=N1TBDMS694.2218Standard non polar3583.903
RI017080152-(alpha-hydroxyethyl)thiamine diphosphate,3TMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS682.1674Standard non polar3312.3108
RI017080142-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#2JsmolCC1=NC=C(C[N+]2=C(C(C)O)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS610.1279Standard non polar3411.9688
RI017080132-(alpha-hydroxyethyl)thiamine diphosphate,2TMS,isomer#1JsmolCC1=NC=C(C[N+]2=C(C(C)O[Si](C)(C)C)SC(CCOP(=O)([O-])OP(=O)([O-])[O-])=C2C)C(N[Si](C)(C)C)=N1TMS610.1279Standard non polar3225.6335
RI017080122,6-diamino-4-hydroxy-5-formamidopyrimidine,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C=O)[C-]1C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[N+]=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS738.4845Standard polar3348.39
RI017080112,6-diamino-4-hydroxy-5-formamidopyrimidine,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)[C-](N(C=O)[Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=[N+]1TBDMS624.3981Standard polar3630.577
RI017080102,6-diamino-4-hydroxy-5-formamidopyrimidine,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=[N+]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)[C-]1N(C=O)[Si](C)(C)C(C)(C)CTBDMS624.3981Standard polar3496.1792
RI017080092,6-diamino-4-hydroxy-5-formamidopyrimidine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)[C-](NC=O)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=[N+]1)[Si](C)(C)C(C)(C)CTBDMS624.3981Standard polar3834.0134
RI017080082,6-diamino-4-hydroxy-5-formamidopyrimidine,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N(C=O)[C-]1C(=O)N=C(N)[N+]=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS510.3116Standard polar3752.2751
RI017080072,6-diamino-4-hydroxy-5-formamidopyrimidine,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C=O)[C-]1C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[N+]=C1NTBDMS510.3116Standard polar3692.2551
RI017080062,6-diamino-4-hydroxy-5-formamidopyrimidine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)[C-](NC=O)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=[N+]1TBDMS510.3116Standard polar4038.87
RI017080052,6-diamino-4-hydroxy-5-formamidopyrimidine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)[C-](N(C=O)[Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=[N+]1TBDMS510.3116Standard polar3769.2327
RI017080042,6-diamino-4-hydroxy-5-formamidopyrimidine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=[N+]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)[C-]1NC=OTBDMS510.3116Standard polar3942.8176
RI017080032,6-diamino-4-hydroxy-5-formamidopyrimidine,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)NC1=[N+]C(N)=NC(=O)[C-]1N(C=O)[Si](C)(C)C(C)(C)CTBDMS396.2251Standard polar3826.4895
RI017080022,6-diamino-4-hydroxy-5-formamidopyrimidine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C1=[N+]C(N)=NC(=O)[C-]1NC=O)[Si](C)(C)C(C)(C)CTBDMS396.2251Standard polar3985.049
Displaying retention index compounds 16151 - 16175 of 1722868 in total