1-bromononane

CCCCCCCC=Cc1cccc(OC)c1
Reaction #46727
pure product
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCN1C(=O)N(c2ccc([N+](=O)[O-])c(C(F)(F)F)c2)C(=O)C1(C)C
Reaction #64216
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCCCCN1C(=O)N(c2ccc([N+](=O)[O-])c(C(F)(F)F)c2)C(=O)C1(C)C
Reaction #64217
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCCCCOCCCCO
Reaction #64413
4-nonyloxybutanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCCCCCc1cc(C)c2c(n1)N(C)CC2
Reaction #88673
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCCCCCCCCCCCc1cc(C)c2c(n1)N(C)CC2
Reaction #88677
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCCCCOc1cccc(Cl)c1C=O
Reaction #224763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCn1cc(CN(C(=O)C2CCCc3c(OCc4ccccc4)cccc32)c2ccc(C(C)C)nc2)cn1
Reaction #252639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCOc1cc(C(=O)Nc2c(Cl)cncc2Cl)ccc1OC
Reaction #263929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCn1cc(CN(C(=O)C2CCCc3c(OCc4ccccc4)cccc32)c2ccc(C(C)C)nc2)cn1
Reaction #305969
5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-[(1-nonylpyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCCCCCCCCOC(=O)c1c[nH]c2ccccc12
Reaction #348014
nonyl indole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
CCCCCCCCCOC(=O)c1cc(-c2csc(-c3ccc(OCC)c(OCC)c3)n2)ccc1OCOC
Reaction #350778
2-(3,4-diethoxyphenyl)-4-(3-nonyloxycarbonyl-4-methoxymethoxyphenyl)thiazole
Rendimiento 43.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)nc(N)nc21
Reaction #351902
mixture
Rendimiento 39.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCCCCOc1ccc(-c2cnc(-c3ccc(CCCCCC)cc3)cn2)cc1F
Reaction #381039
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCCCOc1ccccc1C=O
Reaction #417292
2-nonyloxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CCCCCCCCCOc1cccc(Cl)c1C=O
Reaction #417297
2-chloro-6-nonyloxy benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)nc(N)nc21
Reaction #429099
mixture
Rendimiento 39.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)ncnc21
Reaction #430073
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCCCCCCN1C(=O)N(c2ccc([N+](=O)[O-])c(C(F)(F)F)c2)C(=O)C1(C)C
Reaction #442768
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CCCCCCCCCN1C(=O)N(c2ccc([N+](=O)[O-])c(C(F)(F)F)c2)C(=O)C1(C)C
Reaction #442769
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
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