2-ethylhexyl bromide

CCCCC(CC)COCCCCCCCCCCO
Reaction #1192
10-(2-ethylhexyloxy)decanol
Rendimiento 72.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(CC)COc1ccc(OC)cc1
Reaction #50162
1-methoxy-4-(2'-ethylhexyloxy)benzene
Rendimiento 43.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCCCC(CC)COc1c(I)cc(I)cc1I
Reaction #81760
2-ethyl-1-(2,4,6-triiodophenoxy)-hexane
Rendimiento 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCC(CC)COc1ccc(C#N)cc1
Reaction #203896
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC(CC)COc1ccc(Br)cc1
Reaction #259076
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC(CC)COc1c(I)cc(I)cc1I
Reaction #297543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCC(CC)COc1ccc(C#N)cc1
Reaction #320079
4-(2-ethylhexyloxy)benzonitrile
Rendimiento 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCC(CC)COc1ccc(-c2nc(-c3ccc(OCC(CC)CCCC)cc3)nc(-c3ccc(OCC(CC)CCCC)cc3O)n2)cc1
Reaction #320080
red-brown oil
Rendimiento 101.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCC(CC)COc1ccc(Br)cc1
Reaction #320082
4-(2-ethylhexyloxy)bromobenzene
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCC(CC)COc1ccc2cccc(NC(C)=O)c2c1
Reaction #335980
1-acetamino-7-(2-ethylhexyloxy)naphthalene
Rendimiento 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCC(CC)COc1ccc(C(=O)OC)c(O)c1
Reaction #351531
methyl 4-(2-ethylhexyloxy)-2-hydroxybenzoate
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCC(CC)COc1ccc2c(c1)C(=O)c1ccc(OCC(CC)CCCC)cc1C2=O
Reaction #366019
product
Rendimiento 128.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCCC(CC)CC1(CC(CC)CCCC)c2cc(Cl)ccc2-c2ccc(Cl)cc21
Reaction #366601
2,7-dichloro-9,9-di(2-ethylhexyl)-fluorene
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCCC(CC)CC#N
Reaction #373987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)CN1C(=O)C2CC2C1=O
Reaction #379722
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)COc1ccc(-c2nc(-c3ccc(OCC(CC)CCCC)cc3)nc(-c3ccc(OCC(CC)CCCC)cc3O)n2)cc1
Reaction #382116
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)CN1C=C(C(C)=O)CCC1
Reaction #384431
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)COCCCCCCCCCCO
Reaction #386685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)COc1ccc(C(=O)OC)c(O)c1
Reaction #391998
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC(CC)CN(CCCCCC(=O)OC)c1ccccc1
Reaction #407106
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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