methyl β-hydroxyethyl ketone

CC(O)(CCO)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55206
3-(2',4'-difluoro-4-biphenylyl)butane-1,3-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1=C(C)C(=O)C(C)CC1
Reaction #94084
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC1=C(C)C(=O)C(C)CC1
Reaction #94087
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC(=O)CCOc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(-c2ccc(F)cc2)c1=O
Reaction #187922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)(CCO)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #280242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)CCOC(C)=O
Reaction #288859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC1(C)CCc2c(C)c(O)c(C)c(C)c2O1
Reaction #355587
(±)-6-hydroxy-2-methoxy-2,5,7,8-tetramethylchroman
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CC(CCO)(C[N+](=O)[O-])SCc1ccccc1
Reaction #389862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC1(C)CCc2c(C)c(O)c(C)c(C)c2O1
Reaction #416022
(±)-6-hydroxy-2-methoxy-2,5,7,8 -tetramethylchroman
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CC(=O)CCOc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(-c2ccc(F)cc2)c1=O
Reaction #469169
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC(CCO)(C[N+](=O)[O-])SCc1ccccc1
Reaction #591813
title compound
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(=O)CCn1nc(-c2ccccc2)c2c(Cl)c(-c3ccccc3)nnc21
Reaction #675791
4-(4-chloro-3,5-diphenyl-pyrazolo[3,4-c]pyridazin-1-yl)butan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)CCOCc1cc2ccccc2oc1=O
Reaction #679307
3-(3-oxo-butoxymethyl)-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)CCOC(=O)c1cc2ccccc2oc1=O
Reaction #679309
2-oxo-2H-chromene-3-carboxylic acid 3-oxo-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)CCO[Si](C)(C)C(C)(C)C
Reaction #692615
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Cc1cc(-c2ccc3c(c2)CCN(C(C)CCO)CC3)n(C)n1
Reaction #782113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(CCO)N1CCc2cc3nc(C(F)(F)F)oc3c(Br)c2CC1
Reaction #893104
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(=O)CCOc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(-c2ccc(F)cc2)c1=O
Reaction #978589
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
CC(=O)CCOC(=O)c1ccccc1
Reaction #1004579
3-oxobutylbenzoate
Выход 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
CC(CCO)Nc1cccc(C2=C(c3cn(C)c4ccccc34)C(=O)NC2=O)c1
Reaction #1104763
3-(1-methylindol-3-yl)-4-[3-(3-hydroxy-1-methylpropylamino)phenyl]-1H-pyrrole-2,5-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
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