1-(4-chlorophenyl)ethanone

CN(C)CCC(=O)c1ccc(Cl)cc1.Cl
Reaction #40770
product
المردود 112.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(/C=C/c2ccccc2)cc1
Reaction #42156
(trans)-4-acetylstilbene
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(/C=C/c2ccccc2)cc1
Reaction #42175
(trans)-4-acetylstilbene
المردود 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)/C=C/C(=O)c1ccc(Cl)cc1
Reaction #61719
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C)/C=C/C(=O)c1ccc(Cl)cc1
Reaction #61728
title compound
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)c1ccc(SCCCCO)cc1
Reaction #61736
1-[4-(4-hydroxybutylsulfanyl)phenyl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(Cc1cc(C(F)(F)F)ns1)c1ccc(Cl)cc1
Reaction #65222
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
NCC1CCN(CCOc2cccc(Cl)c2)CC1
Reaction #183303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(C=Cc2ccccc2)cc1
Reaction #189686
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
Reaction #193272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(SCCCCO)cc1
Reaction #194212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCC(=O)CC(=O)c1ccc(Cl)cc1
Reaction #196491
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2c(c1)COc1ccccc1-2
Reaction #204608
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CC(=O)C(F)F)c1ccc(Cl)cc1
Reaction #216385
yellow solid
المردود 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
Reaction #216386
yellow solid
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Cc1cc(C=CC(=O)c2ccc(Cl)cc2)cc(C)c1O
Reaction #219263
1-[4-chlorophenyl]-3-[3,5-dimethyl-4-hydroxyphenyl]prop-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
Reaction #242817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(c2ccc(Cl)cc2)CO1
Reaction #255115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1ccc(-c2cccc(C)c2)cc1
Reaction #315035
white solid
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cc(C=CC(=O)c2ccc(Cl)cc2)cc(C)c1O
Reaction #317755
1-[4-chlorophenyl]-3-[3,5-dimethyl-4-hydroxyphenyl]prop-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
الصفحة 1التالي