Ähnlichkeitssuche

CCCCNCCCC

CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #3029
N,N-dioctadecyl-2,4-dinitrobenzenamine
Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)CCCOc1ccc(-c2cn3ccccc3n2)cc1
Reaction #4823
title compound
Ausbeute 192.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)CCCOc1ccc(-c2nc3c(C)cccn3c2C)cc1
Reaction #4824
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)CCCOc1ccc(C(=O)c2cn3cccc(C)c3n2)cc1
Reaction #4825
title compound
Ausbeute 197.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #4826
free base
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCCO)c1ccc(C=O)cc1
Reaction #6296
4-(N-4-hydroxybutyl-N-butylamino)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CCCCCN(CCCCC)c1ccc2nc3ccc(N(CCC)CCC)cc3[s+]c2c1.[I-]
Reaction #42647
3-(N,N-dipentylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(CCCCCC)c1ccc2nc3ccc(N(CCC)CCC)cc3[s+]c2c1.[I-]
Reaction #42648
3-(N,N-dihexylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1
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
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C=O)CCCCCCCCC
Reaction #43899
α-methylene undecanal
Ausbeute 1583.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C=O)CCCCCC
Reaction #43900
a-methylene octanal
Ausbeute 1636.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C=O)C(C)CCCC(C)(C)O
Reaction #43901
3,7-dimethyl-2-methylene-7-hydroxyoctanal
Ausbeute 1341.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46027
fatty acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(CCCCCC)C1=NS(=O)(=O)N=C1OCC
Reaction #46328
title intermediate
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49204
amide
Ausbeute 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49207
amide
Ausbeute 172.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64010
oil
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCSC1c1nsc2ccc(-n3c(=O)cc(C(F)(F)F)n(C)c3=O)cc12
Reaction #77290
title compound
Ausbeute 31.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)c1ccc([N+](=O)[O-])cc1F
Reaction #84418
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter