1,4-butane sultone

Cc1nc2c(CCCCS(=O)(=O)O)cccc2s1
Reaction #45207
Compound 1
收率 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)C(C)CCCCS(=O)(=O)O
Reaction #68705
5-Methyl-6-oxoheptane-1-sulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1N(CCCCS(=O)(=O)O)c2ccc3ccccc3c2C1(C)C
Reaction #163304
3-(4-Sulfobutyl)-1,1,2-trimethyl-1H-benzo[e]indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1sc2cc(S(=O)(=O)N(C)C)ccc2[n+]1CCCCS(=O)(=O)[O-]
Reaction #171965
Compound 26
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(C2C(CCC(O)c3ccc(F)cc3F)C(=O)N2c2ccc(OCCCCS(=O)(=O)O)cc2)cc1
Reaction #219931
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C1C(CCC(O)c2ccc(F)cc2)C(c2ccc(OCCCCS(=O)(=O)O)cc2)N1c1ccc(F)cc1
Reaction #219932
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=C(C)C(=O)NCCC[N+](C)(C)CCCCS(=O)(=O)[O-]
Reaction #324369
4-sulfonatobutyl[3-(methacryloylamino)propyl]dimethylammonium
收率 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCC[n+]1ccn(C)c1.O=S(=O)([O-])CCCCCl
Reaction #326378
1-butyl-3-methylimidazolium 4-chlorobutylsulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)NCCCCS(=O)(=O)O
Reaction #326915
4-(tert-butylamino)-1-butanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)NCCCCS(=O)(=O)O
Reaction #326977
4-(tert-butylamino)-1-butanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCNCCCCS(=O)(=O)O
Reaction #326979
4-(ethylamino)-1-butanesulfonic acid
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCCCCCCNCCCCS(=O)(=O)O
Reaction #326981
4-(octylamino)-1-butanesulfonic acid
收率 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc(CNC(C)CCS(=O)(=O)O)cc1OC
Reaction #326983
3-[(3,4-dimethoxybenzyl)amino]-1-butanesulfonic acid
收率 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=S(=O)(O)CCCCNC1C2CC3CC(C2)CC1C3
Reaction #326984
4-(2-adamantyl)amino-1-butanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=S(=O)(O)CCCCNC1CCCCC1
Reaction #326990
4-(cyclohexylamino)-1-butanesulfonic acid
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1ccc2c(ccc(C)[n+]2CCCCS(=O)(=O)[O-])c1
Reaction #346849
4-[2,6-dimethyl-1-quinolinio]butane sulfonate
收率 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
Cc1ccc2c(ccc(C)[n+]2CCCCS(=O)(=O)[O-])c1
Reaction #361382
4-[2,6-dimethyl-1quinolinio]butanesulfonate
收率 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
O=S(=O)(O)CCCCN1CCOCC1
Reaction #411183
title compound
收率 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COc1ccc(C2C(CCC(O)c3ccc(F)cc3F)C(=O)N2c2ccc(OCCCCS(=O)(=O)O)cc2)cc1
Reaction #434972
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
O=C1C(CCC(O)c2ccc(F)cc2)C(c2ccc(OCCCCS(=O)(=O)O)cc2)N1c1ccc(F)cc1
Reaction #434973
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
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