Substructure Search

7731

Br.COc1cnccc1C(=O)CBr
Reaction #4454
α-bromo-3-methoxy-4-acetylpyridine hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
COC1=Cc2ccccc2Nc2ccccc21
Reaction #9811
10-methoxy-5H-dibenz[b,f]azepine
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1c2ccccc2CC(=O)c2ccccc21
Reaction #9812
oxcarbazepine
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC/C=C/CCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9885
(S)-trans-1-dec-4-enyl-3-(1-methyl-pyrrolidin -2-yl)-1-pyridinium bromide
Yield 74.1%DOI: 10.6084/m9.figshare.5104873.v1
Br.CCCCC/C=C\CCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9889
(S)-cis-1-dec-4-enyl-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9892
(S)-1-dec-9-enyl-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9895
(S)-3-(1-methyl-pyrrolidin-2-yl)-1-undec-10-enyl-pyridinium bromide
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1CCC[C@H]1c1ccc[n+](CCCCCCC2CCC2)c1.[Br-]
Reaction #9900
(S)-1-(6-cyclobutyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC#CCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9913
(S)-1-dec-3-ynyl-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide
Yield 51.8%DOI: 10.6084/m9.figshare.5104873.v1
Br.CC(C)=CCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9917
(S)-1-(7-Methyl-oct-6-enyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Br.CC(C)CCCCCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9920
(S)-1-(7-Methyl-octyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCOCC[n+]1cccc([C@@H]2CCCN2C)c1.[Br-]
Reaction #9921
(S)-1-[2-(2-ethoxy-ethoxy)-ethyl]-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(c2cccc[n+]2[O-])c2cc([N+](=O)[O-])ccc2O1
Reaction #65384
2-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(c2cccc[n+]2[O-])c2ccc([N+](=O)[O-])cc2O1
Reaction #65403
2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide
Yield 23.5%DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc(Cl)c(Br)c1
Reaction #67607
3-bromo-4-chloro-pyridine-N-oxide
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[n+]1ccccc1)c1ccccc1.[Br-]
Reaction #75290
N-phenacylpyridinium bromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[n+]1ccccc1)c1ccccc1.[Br-]
Reaction #75291
N-phenacylpyridinium bromide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c[nH]c(=O)cc1Br
Reaction #84998
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1-c1cc(=O)[nH]cc1C(F)F
Reaction #85006
4-Chloro-2-[5-(difluoromethyl)-2-oxo-1,2-dihydropyridin-4-yl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1c[nH]c(=O)cc1Br
Reaction #85113
4-Bromo-5-methoxypyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
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