1-bromo-2-(2-bromoethyldisulfanyl)ethane

Cc1n(C)c2ccccc2[n+]1CCSSCC[n+]1c(C)n(C)c2ccccc21.[Br-].[Br-]
Reaction #40263
3,3′-(disulfanediyldiethane-2,1-diyl)bis(1,2-dimethyl-1H-benzimidazol-3-ium) dibromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #507594
light beige product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
Reaction #507596
expected product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #742267
light beige product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #1130532
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
Reaction #1130535
expected product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #1751260
light beige product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #1751262
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
Reaction #1751265
expected product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #2278355
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_12
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
Reaction #2278358
expected product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_12
Cc1cccc[n+]1CCSSCC[n+]1ccccc1C.[Br-].[Br-]
Reaction #2446056
1,1′-(Disulphanediyldiethane-2,1-diyl)bis(2-methylpyridinium)dibromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
Cc1cc[n+](CCSSCC[n+]2ccc(C)cc2)cc1.[Br-].[Br-]
Reaction #2446059
expected product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04