cyclohexa-2,5-diene-1,4-dione

O=C1C=CC(=O)C2=C1CC=CC2
Reaction #64367
title compound
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC1=C(C)CC2=C(C1)C(=O)C=CC2=O
Reaction #64368
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
—
Reaction #65126
( II )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C1C=CC(=O)c2cc3sc(=S)sc3cc21
Reaction #69883
2-thioxonaphth[2,3-d] [1,3]dithiol-5,8-dione
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C=CC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74961
1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Oc1ccc(O)c2c1C1(Br)C(Br)=C(Br)C2(Br)C1(Br)Br
Reaction #74967
1,2,3,4,9,9-hexabromo-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(=O)CC(=O)CC(=O)O
Reaction #90844
triacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Oc1ccc2c(-c3ccncc3)c3n(c2c1)CCCCC3
Reaction #95101
7,8,9,10-Tetrahydro-11-(4-pyridyl)-6H-azepino[1,2-a]indole-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=[N+]([O-])c1cc([N+](=O)[O-])c(C=Cc2c([N+](=O)[O-])cc([N+](=O)[O-])cc2[N+](=O)[O-])c([N+](=O)[O-])c1
Reaction #191081
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC1(CC(C)=O)Cc2cc(OC)ccc2C1=O
Reaction #195698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1ccc2nc3ccccc3sc-2c1
Reaction #318222
3H-phenothiazin-3-one
Yield 62.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCOC(=O)c1c(C)n(C2CC2)c2ccc(O)cc12
Reaction #337431
title compound
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(CC(OC)OC(C)=O)OC
Reaction #364746
1,1,3-Trimethoxy-3-acetoxypropane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=C1C=CC(=O)C=C1
Reaction #388578
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC1(CC(C)=O)CCc2cc(OC)ccc2C1=O
Reaction #389159
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=Cc1ccccc1C=C
Reaction #409783
divinylbenzene
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Nc1nc2ccc(O)cc2s1
Reaction #420898
2-amino-1,3-benzothiazol-6-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C1C=CC(=O)C(SCCO)=C1
Reaction #431746
2-(β-hydroxyethylthio)-1,4-benzoquinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
O=C1C=C(SCCO)C(=O)C=C1SCCO
Reaction #431748
2,5-bis-(β-hydroxyethylthio)-1,4benzoquinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CC1(C)c2cc(O)ccc2OC1N1CCCCC1
Reaction #459590
2,3-dihydro-3,3-dimethyl-5-hydroxy-2-piperidino-benzofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
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