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CC(=O)CCO

O=C1C=CC(OC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #2659
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1C=C[C@H](OC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #2660
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(CC(O)C(CCCCCC)C(=O)OC)OC1CCCCO1
Reaction #6149
methyl 2-hexyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N2CCC[C@H]2C1
Reaction #9984
title compound
Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1C(=O)c2cc3ccccc3cc2C1=O)C(C)=O
Reaction #10976
Methyl 2-(1,3-dioxo-1,3-dihydro-benzo[f]isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(COC(C)=O)C(C)=O
Reaction #40764
light-yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN=C1CCOCC1
Reaction #41159
N′-(tetrahydro-pyran-4-ylidene)-hydrazinecarboxylic acid tert-butyl ester
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1OC12CCOCC2
Reaction #48663
desired compound
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)C(CC1(C(=O)O)CCCC1)C(=O)OC(C)(C)C
Reaction #51189
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#Cc1ccc2ccccc2c1
Reaction #52296
naphthalene-2-yl-propynoic acid ethyl ester
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2nc(NC(C)(C)C)c(F)cc2F)c2c(Br)c(F)c(F)cc2c1=O
Reaction #53451
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2ccc3ccccc3c2)c2ccc(O)cc2o1
Reaction #54577
7-hydroxy-4-(2-naphthyl)coumarin
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C(C)C)C(c1ccc(F)cc1)C1CCCCC1=O
Reaction #57365
methyl 4-fluoro-α-(1-oxo-2-methylpropyl)-β-(2-oxocyclohexyl)benzenepropanoate
DOI: 10.6084/m9.figshare.5104873.v1
OCC1COC2(CCOCC2)OC1
Reaction #59886
title compound
Ausbeute 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63423
desired compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63424
desired compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C=CC(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1)C(=O)OC
Reaction #63426
faint yellow crystalline desired compound
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2cc(OC)ccc2c1O
Reaction #63942
final product
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(c1c(OC)nn2c(-c3c(OC)cc(OCC)cc3OC)csc12)C1CCOCC1
Reaction #69557
title compound
Ausbeute 59.6%DOI: 10.6084/m9.figshare.5104873.v1
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