sodium thiocyanate

N#CSCc1ccc(C(=O)c2ccc(Cl)cc2)cc1
Reaction #2198
desired product
Rendement 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNC(=O)c1cc(Oc2ccc3c(c2)nc(NC(=O)c2ccc(CCl)cc2)n3C)ccn1
Reaction #41751
[4-(2-{[4-(chloromethyl)phenyl]carbonylamino)-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Nc1nc2ccc(Oc3nccc(-c4cccnc4)n3)cc2[nH]1)c1ccc(CCl)cc1
Reaction #41755
[4-(chloromethyl)phenyl]-N-[5-(4-(3-pyridyl)pyrimidin-2-yloxy)benzimidazol-2-yl]carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCCCC1CNC(N)=S
Reaction #46374
title product
Rendement 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)c1cc(N)c([N+](=O)[O-])cc1SC#N
Reaction #51762
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cccnc1C(=O)c1cc(N)c(F)cc1SC#N
Reaction #77253
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)Cn1c2c(c(=O)[nH]c1=S)CCC2
Reaction #91298
title compound
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(SC#N)ccc1O
Reaction #157256
3-methyl-4-hydroxy-phenyl thiocyanic acid
Rendement 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1cc(SC#N)ccc1O
Reaction #157263
3-ethyl-4-hydroxy-phenyl thiocyanic acid
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1[nH]cnc1-c1ccccc1
Reaction #327988
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
N#CSc1ccc(C=O)n1-c1ncccc1Cl
Reaction #339187
1-(3-chloro-2-pyridinyl)-5-thiocyanato-1H-pyrrole-2-carbaldehyde
Rendement 125.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
N#CSc1ccc(N)c([N+](=O)[O-])c1
Reaction #345941
2-nitro-4-thiocyanato-aniline
Rendement 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
CC(=O)C(CCCl)SC#N
Reaction #352819
3-thiocyanato-5-chloro-2-pentanone
Rendement 96.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=O)C(CCCl)SC#N
Reaction #352821
3-thiocyanato-5-chloro-2-pentanone
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Cc1nc(Cl)sc1CCCl
Reaction #352825
2-chloro-4-methyl-5-(2-chloroethyl)-thiazole
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
N#CSC(C(=O)O)c1ccc(-c2ccccc2Cl)cc1
Reaction #354576
α-thiocyanato-2'-chloro-4-biphenylylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
O=C(Cc1ccc(F)cc1)NC(=S)Nc1ccc(Oc2ncnn3cccc23)c(F)c1
Reaction #434667
title compound
Rendement 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(C)c1ccn2c1C(Oc1ccc(NC(=S)NC(=O)Cc3ccc(F)cc3)cc1F)NC=N2
Reaction #434693
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCN(CC)C(=O)SC#N
Reaction #441164
N,N-Diethyl carbamoyl thiocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CC(C)c1cc(Oc2ccccc2)cc(C(C)C)c1NC(N)=S
Reaction #446013
N-(4-phenoxy-2,6-diisopropylphenyl)thiourea
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
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