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11314

NCC(O)CNC(=O)CCCCCCCCCCCO
Reaction #1220
title compound
Выход 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
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
Выход 112.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H](O)CC(=O)O
Reaction #5718
(R)-3-hydroxytetradecanoic acid
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCCCCCC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6161
N-formyl-L-leucine (S)-1-[[(2S,3S)-3-decyl-4-oxo-2-oxetanyl]methyl]-4-pentenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCc1c([N+](=O)[O-])cc([N+](=O)[O-])c(OCC)c1C1C(C(=O)OCC)=C(C)NC(C)=C1C(=O)OCC
Reaction #52059
diethyl 1,4-dihydro-4-(2′-ethoxy-3′,5′-dinitro-6′-pentadecylphenyl)-2,6-dimethyl-3,5-pyridine dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](CCCCCOS(C)(=O)=O)CC1
Reaction #53872
trans-Methansulfonic acid 5[-4-(tert-butoxy carbonyl-methyl-amino)-cyclohexyl)-pentylester
Выход 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CC[C@H](CCCCCOS(C)(=O)=O)CC1
Reaction #53873
trans-Methansulfonic acid 5-(4-methyl amino-cyclohexyl)-pentylester
Выход 166.6%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
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55563
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Выход 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55564
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Выход 94.0%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
Выход 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
Выход 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
Выход 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](O)C(C)C(=O)OC
Reaction #64087
methyl (3S)-2-methyl-3-hydroxypentanoate
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1
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