Recherche de Sous-structure

CCCCCCCCCCCCO

NCC(O)CNC(=O)CCCCCCCCCCCO
Reaction #1220
title compound
Rendement 75.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCC(=O)OC(C)C
Reaction #1500
isopropyl myristate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC[n+]1ccn(C)c1.[Cl-]
Reaction #4815
1-n-Dodecanoyloxymethyl-3-Methylimidazolium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC[N+]12CCC(CC1)CC2.[Cl-]
Reaction #4816
n-Dodecanoyloxymethylquinuclidinium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC
Reaction #4991
Dodecyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)O
Reaction #5384
Oleic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccccc1
Reaction #5717
methyl (R)-3-(benzyloxy)-tetradecanoate
Rendement 112.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H](O)CC(=O)O
Reaction #5718
(R)-3-hydroxytetradecanoic acid
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCNC(=O)C(F)(F)F
Reaction #11999
amide
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1(CC[C@@H]2[C@H]3CC(=O)O[C@H]3C[C@H]2O)OCCO1
Reaction #50197
title compound ( 6a )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1(CC[C@@H]2[C@H]3CC(=O)O[C@H]3C[C@H]2OC2CCCCO2)OCCO1
Reaction #50198
title compound ( 59 )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOc1nc(OCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54159
6-(4-hydroxy-3,5-diphenylphenoxy)-2,4-dilauroxys-triazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOc1nc(OCCCCCCCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54160
6-(4-hydroxy-3,5-diphenyphenoxy)-2,4-distearoxy-s-triazine
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C2C[C@H]3[C@@H]4N(C)c5ccccc5C45C[C@@H](C2[C@H]5O)[N+]3([O-])[C@@H]1O
Reaction #54463
N-oxy-ajmaline
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(O)C1
Reaction #62539
menthol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64079
t-butyl (3S)-2-methyl-3-hydroxybutanoate
Rendement 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64085
t-butyl (3S )-2-ethyl-3-hydroxybutanoate
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64086
t-butyl (3S)-2-allyl-3-hydroxybutanoate
Rendement 45.3%DOI: 10.6084/m9.figshare.5104873.v1
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