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CCC(=O)O

CCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5342
4-hydroxy-3-((Z)-1-oxo-9-tetradecenyl)-2(5H)-furanone
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5343
4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC#CCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5344
4-hydroxy-3-(1-oxo-9-octadecynyl)-2(5H)-furanone
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5345
4-hydroxy-3-(1-oxooctadecyl)-2(5H)-furanone
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5367
4-hydroxy-3-[1-oxohexadecyl]-2(5H)-furanone
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1CC(=O)O
Reaction #52584
2-methyl-6-nitrophenylacetic acid
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)CC1
Reaction #53155
(Z)-3-{1-[4-(4-ethoxycarbonyl-piperidinomethyl)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65578
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65579
3-(3-Cyclododecyl-1-oxopropyl)-4-hydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65588
4-Hydroxy-2-oxo-2.5-dihydro-furan-3-carboxylic acid-2-cyclododecyl-ethylamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80793
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
Выход 78.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80794
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(c2ccc(Br)cc2)CC1
Reaction #85866
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CSC(c2ccccc2O)N1C(=O)CCBr
Reaction #96278
product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCSSCCC(=O)N1C(c2ccccc2O)SC[C@H]1C(=O)O
Reaction #96279
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](N)CS.Cl
Reaction #96280
L-cysteine ethyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #158498
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)Cc1ccc2c(c1)CCCN2
Reaction #162000
#215
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #163608
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Nc1ccccc1)c1ccccc1
Reaction #164147
pale yellow solid
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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