参与 10 个反应

8107

CCCCCCCCc1ccc(-c2ccc(O)cc2)nc1
Reaction #4027
2-(p-hydroxyphenyl)-5-octylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCc1ccc(-c2ccc(OCCC[C@H](C)CCCCCC)cc2)nc1
Reaction #4028
(R)2-[p-(4-methyldecyloxy)phenyl]-5-octylpyridine
收率 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCc1ccc(-c2ccc(OCCCC(C)CCCCCC)cc2)nc1
Reaction #174140
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCc1ccc(-c2ccc(OC(=O)CCCCCC)cc2)nc1
Reaction #375620
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCCc1ccc(-c2ccc(O)cc2)nc1
Reaction #1204502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCCCCCCCc1ccc(-c2ccc(O)cc2)nc1
Reaction #1286016
p-(5-octyl-2-pyridyl)phenol
收率 35.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
CCCCCCCCc1ccc(-c2ccc(OCCCCC[C@@H](C)CC)cc2)nc1
Reaction #1286017
(S)-2-[p-(6-methyloctyloxy)phenyl]-5-octylpyridine
收率 23.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
CCCCCCCCc1ccc(-c2ccc(OCCCCCC(C)CC)cc2)nc1
Reaction #1327243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCCCCCCc1ccc(-c2ccc(OC(=O)CCCCCC)cc2)nc1
Reaction #1579149
4-(5-octyl-2-pyridyl)phenyl heptanoate
收率 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_12
CCCCCCCCc1ccc(-c2ccc(O)cc2)nc1
Reaction #1641877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)