Participa en 347 reacciones

CCCCNCCCC

CCCCN(CCCC)CCCOc1ccc(-c2cn3ccccc3n2)cc1
Reaction #4823
title compound
Rendimiento 192.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCN(CCCC)CCCOc1ccc(-c2nc3c(C)cccn3c2C)cc1
Reaction #4824
title compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCN(CCCC)CCCOc1ccc(C(=O)c2cn3cccc(C)c3n2)cc1
Reaction #4825
title compound
Rendimiento 197.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #4826
free base
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCN(CCCC)c1ccc2nc3ccc(N(CCC)CCC)cc3[s+]c2c1.[I-]
Reaction #42646
3-(N,N-dibutylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C=O)=CCC1CC=C(C)C1(C)C
Reaction #43898
2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-but-2-en-1-al
Rendimiento 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C(C=O)CCCCCCCCC
Reaction #43899
α-methylene undecanal
Rendimiento 1583.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C(C=O)CCCCCC
Reaction #43900
a-methylene octanal
Rendimiento 1636.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C(C=O)C(C)CCCC(C)(C)O
Reaction #43901
3,7-dimethyl-2-methylene-7-hydroxyoctanal
Rendimiento 1341.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(CCCC)c1ccc([N+](=O)[O-])cc1F
Reaction #84418
title compound
Rendimiento 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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Reaction #89604
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCN(CCCC)C(=O)c1nn(-c2ccc(Cl)cc2)c(C)cc1=O
Reaction #95544
product
Rendimiento 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCN(CCCC)c1c(OC)cccc1OC
Reaction #172485
4-dibutylamino-3,5-dimethoxybenzene
Rendimiento 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCN(CCCC)Cc1nc(-c2ncn3c2CN(C)C(=O)c2cc(F)ccc2-3)no1
Reaction #186302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCN(CCCCC)CCCOc1ccc(-c2cn3cccc(C)c3n2)cc1
Reaction #199314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC(C=O)=CC(=O)OC
Reaction #201243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN(CCCC)C(=O)COCc1ccccc1
Reaction #206379
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN(CCCC)Cc1nc(-c2ncn3c2C2CCN2C(=O)c2c-3ccc(F)c2Cl)no1
Reaction #209966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOC(=O)/C=C(/C)C=O
Reaction #214929
3-formyl-crotonic acid butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCN(CCCC)p1oc2c(C(C)(C)C)cc(C(C)(C)C)cc2c2cc(C(C)(C)C)cc(C(C)(C)C)c2o1
Reaction #215548
N-(2,4,8,10-tetra-tert-butyl-dibenz[d,f][1,3,2]dioxaphosphepin-6-yl)-dibutylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
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