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10795

CCOC(=O)ONC(=N)c1ccccc1-c1ccc(Cn2c(OCC)nc3cccc(C(=O)OC)c32)cc1
Reaction #5337
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C#C[Si](C)(C)C)(OCC)OCC
Reaction #52306
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55215
3-(2',4'-difluoro-4-biphenylyl)butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])C(F)(COC(OCC(F)([N+](=O)[O-])[N+](=O)[O-])(OCC(F)([N+](=O)[O-])[N+](=O)[O-])OCC(COCOCC(CO)([N+](=O)[O-])[N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
Reaction #334416
mono-orthocarbonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)NC(=O)c1ccc2oc(OCC)nc2c1
Reaction #426524
2-Ethoxy-benzooxazole-5-carboxylic acid (1-propyl-butyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=NS(=O)(=O)C(F)(c2cccc(Br)c2)C(C)(C)O1
Reaction #427062
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=NS(=O)(=O)C(c2ccc(-c3ccccc3)cc2)C(C)(C)O1
Reaction #427066
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=NS(=O)(=O)C(C)(c2cccc(Br)c2)C(C)(C)O1
Reaction #427073
product
DOI: 10.6084/m9.figshare.5104873.v1
COC1=NS(=O)(=O)C(c2ccc(-c3ccccc3)cc2)C2(COC2)O1
Reaction #427078
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2ccc(OCCCCCC(=O)OC)cc2n1-c1ccccc1
Reaction #547715
6-[[2-Ethoxy-1-phenyl-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2ccc(O)cc2o1
Reaction #555731
2-ethoxy-6-hydroxybenzoxazole
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)(OCC)OCC
Reaction #568329
6
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C1=CCC2(CC1)COC1(OC2)OCC2(CC=CCC2)CO1
Reaction #568332
8,10,19,20-tetraoxatrispiro[5.2.2.5.2.2]henicosa-2,14-diene
DOI: 10.6084/m9.figshare.5104873.v1
CC=CCCCCCCCCCC=CCCCCC
Reaction #568338
nonadeca-2,13-diene
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2ccc(O)cc2o1
Reaction #640170
2-ethoxy-6-hydroxybenzoxazole
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2ccc(O)cc2o1
Reaction #711278
2-ethoxy-6-hydroxybenzoxazole
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c(N)c1C(=O)c1cc(C)ccc1C
Reaction #814579
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2c(C)cc(C)nc2[nH]1
Reaction #972599
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2c(C)ccnc2[nH]1
Reaction #972603
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2cccnc2[nH]1
Reaction #972604
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
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