12-Bromododecan-1-ol

[N-]=[N+]=NCCCCCCCCCCCCO
Reaction #162013
12-Azido-1-dodecanol
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1ccc(OCCCCCCCCCCCCO)cc1
Reaction #204735
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCCCCCCCCCCCCCCCF
Reaction #241064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=CCCCCCCCCCCCBr
Reaction #253694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN1CCN(c2ccc(C(=O)NCCCCCCCCCCCCO)cn2)CC1
Reaction #260766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)CCCCCCCCCCCCCCO
Reaction #285209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CC(=O)OCCCCCCCCCCCCBr
Reaction #351010
12-bromododecyl acrylate
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
BrCCCCCCCCCCCCOCc1ccccc1
Reaction #368455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OCCCCCCCCCCCCSc1nnnn1-c1ccccc1
Reaction #426333
12-(1-phenyl-1H-tetrazol-5-ylsulfanyl)-dodecan-1-ol
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1ccc(CSCCCCCCCCCCCCO)cc1
Reaction #434477
pure product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
Cc1ccc(S(=O)(=O)CCCCCCCCCCCCOC2CCCCO2)cc1
Reaction #527379
12-(4-methylphenyl)sulfonyl-1-tetrahydropyranyloxydodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
BrCCCCCCCCCCCCOC1CCCCO1
Reaction #722972
Tetrahydro-2-(12-bromododecanoxy)-2H pyran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
O=[N+]([O-])c1cc(COCCCCCCCCCCCCO)cc([N+](=O)[O-])c1
Reaction #834659
12-(3,5-dinitrobenzyloxy)-dodecanol
Выход 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
O=C(OCCCCCCCCCCCCBr)C1CC1
Reaction #1059177
cyclopropane carboxylic acid 12-bromododecyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_07
CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OCCCCCCCCCCCCO)C(C)(C)C2)CC(C)(C)N1OCCCCCCCCCCCCO
Reaction #1073067
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
O=Cc1ccc(OCCCCCCCCCCCCO)cc1
Reaction #1074524
4-(12-Hydroxy-dodecyloxy)-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
CCN1CCN(c2ccc(C(=O)NCCCCCCCCCCCCO)cn2)CC1
Reaction #1090485
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
O=C1c2ccccc2C(=O)N1CCCCCCCCCCCCO
Reaction #1090491
title compound
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
OCCCCCCCCCCCCSc1nnnn1-c1ccccc1
Reaction #1112438
12-(1-phenyl-1H-tetrazol-5-ylsulfanyl)-dodecan-1-ol
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
OCCCCCCCCCCCCN1CCOCC1
Reaction #1301089
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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