4-methylphenol

Cc1ccc(OC(=CC(=O)c2ccc(Br)cc2)C(=O)c2ccc(Br)cc2)cc1
Reaction #887
1-(4-tolyloxyl)-1,2-bis(4-bromobenzoyl)ethylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(O)c(C=O)c1
Reaction #1833
product
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C1=C2C3CCC(C3)C2CCC1
Reaction #7365
octahydro-1,4-methanonaphthalene
Yield 145.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc2c(c1)C(c1ccc(OCCO)cc1)C(=O)O2
Reaction #50775
3-[4-(2-hydroxyethoxy)phenyl]-5-methylbenzofuran-2-one
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cc1ccccc1O.N
Reaction #56248
ammonia cresol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)C(Oc1ccc(C)cc1)Oc1ccc(C)cc1
Reaction #56392
Ethyl 2,2-bis(4-methylphenoxy)acetate
Yield 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc(O)c(C(CC(=O)N(C(C)C)C(C)C)c2ccccc2)c1
Reaction #57507
product
Yield 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)Cc1ccccc1Oc1ccc(C)cc1
Reaction #65500
title compound
Yield 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)Oc1ccc(C)cc1
Reaction #73704
p-tolyl acetate
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(OC(=O)c2ccccc2)cc1
Reaction #73709
p-tolyl benzoate
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(OCCO)cc1
Reaction #78790
4-(2-hydroxyethoxy)toluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
—
Reaction #93860
( B )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC(=O)Oc1ccc(CCl)cc1
Reaction #94946
p-acetoxybenzyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C=O.Cc1ccc(O)cc1
Reaction #95441
p-cresol formaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cc1ccc(Oc2ccc(C#N)s2)cc1
Reaction #165097
title compound
Yield 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(Oc2ccc(C#N)s2)cc1
Reaction #173412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC1=C(OC)C(=O)C2=C(CCC(CCOc3ccc(C)cc3)CC2)C1=O
Reaction #180070
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(OCC(=O)c2ccccc2)cc1
Reaction #187794
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Oc1ccc(C)cc1
Reaction #200117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(OCC2CN(C(C)(C)C)C2)cc1
Reaction #203447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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