hexanol

Nc1ccc(Nc2ccccc2)cc1
Reaction #4076
N-phenyl-p-phenylenediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)Nc1ccc(N)cc1
Reaction #4077
N-isopropyl-p-phenylenediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Nc1ccc(NC2CCCCC2)cc1
Reaction #4078
N-cyclohexyl-p-phenylenediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55210
3-(2',4'-difluoro-4-biphenylyl)-butyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCCCOC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Reaction #56256
adenosine-5'-carboxylic acid n-hexyl ester
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCCOc1ccc(Br)cc1-c1cc(Cl)nc(N)n1
Reaction #56915
4-(5-bromo-2-hexyloxy-phenyl)-6-chloro-pyrimidin-2-ylamine
المردود 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1Cc2ccccc2N1
Reaction #77874
2-oxindole
المردود 66.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCCCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C)c1ccccn1.Cl
Reaction #78551
crude product
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCCCO[Si](C)(C)C
Reaction #175143
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1nsnc1-c1cccnc1
Reaction #186467
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc([N+](=O)[O-])cc1C#N
Reaction #192950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #196496
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)CC(OC(=O)Nc2ccccc2)CC(C)(C)N1CC(O)c1ccccc1
Reaction #203484
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #206134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(Nc2ccccc2)cc1
Reaction #208656
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC(=O)C=CCl
Reaction #210666
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)CC(O)CC(C)(C)N1CC(O)c1ccccc1
Reaction #221668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)C1(C)OC2(CC(C)(C)N(CC(O)CO)C(C)(C)C2)NC1=O
Reaction #226836
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOc1nsnc1-c1cccnc1
Reaction #235333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOc1c(F)c(F)c(-c2c(F)c(F)c(C(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F)c(F)c2F)c(F)c1F
Reaction #237259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي