methylcyclohexane

Cc1ccc(C)c(C)c1
Reaction #49636
1,2,4-trimethylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=[N+]([O-])c1ccc2c(c1)C(F)(F)C(F)(F)O2
Reaction #63970
2,3-dihydro-2,2,3,3-tetrafluoro-5-nitrobenzofuran
المردود 311.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCCN(C)C(=O)Cl
Reaction #94616
N-methyl-N-pentylcarbamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
C=C(C)C.C=Cc1ccccc1
Reaction #163425
styrene isobutylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1[nH]c2ccsc2c1C
Reaction #186340
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1OC(Br)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #192759
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1OC(Br)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #196077
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(ON2C(C)(C)CC(OC(=O)c3ccccc3)CC2(C)C)CCCCC1
Reaction #207784
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSc1nnsc1-c1ccc(C(C)(C)C)cc1
Reaction #211648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CN(Cc1ccc(-c2cccc(S(C)(=O)=O)c2)s1)S(=O)(=O)CC1CCCCC1
Reaction #212573
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(c1cccc(O)c1)C(C)CN(C)C
Reaction #230864
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC(CC)COP(=O)([O-])OCC(CC)CCCC
Reaction #235527
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C2(c3ccc(OC)cc3)CC2(Cl)Cl)cc1
Reaction #293094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(C(=O)N2CCO[C@](CCOS(=O)(=O)c3ccc(Cl)cc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314725
title compound
المردود 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1cc(C(=O)N2CCOC(CCOS(=O)(=O)c3ccc(Cl)cc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314726
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)C(C)Oc1ccc(Oc2ncc(Cl)cc2F)cc1
Reaction #319434
solid
المردود 654960.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
C=C(C)C.C=Cc1ccccc1
Reaction #331450
styrene isobutylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)Cc1ccc(SCCN)c(Cl)c1.Cl
Reaction #340344
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)c1ccc(-c2noc3c2CCC(C(=O)O)CC3)cc1
Reaction #369143
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=C(C)C.C=Cc1ccccc1
Reaction #426466
styrene isobutylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
الصفحة 1التالي