Substructure Search

CSCC#N

COc1ccc2[nH]cc(SCC#N)c2c1
Reaction #4408
5-methoxy-3-cyanomethylthioindole
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)CCN
Reaction #6913
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Cl)Sc1cccc(Cl)c1
Reaction #50577
2,3-dichloro-phenylthioacetonitrile
Yield 59.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(CS(=O)(=O)c1ccc(Cl)cc1)NO
Reaction #54436
product
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCOC(=O)c1cccnc1SCC#N
Reaction #55511
cyanomethyl 2-(cyanomethylthio)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)(=O)C(C#N)CCc1ccc(Cl)cc1
Reaction #64920
orange oil
Yield 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CCSC(C#N)=C[C@@H]1[C@@H](C(=O)Cl)C1(C)C
Reaction #69882
(1R)-trans-3-[(1EZ)-2-cyano-2-(ethylthio)ethenyl]-2,2-dimethylcyclopropanecarboxylic acid chloride
Yield 98.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Sc1ccccc1)=C1SCCN1c1ccccc1
Reaction #78235
title compound
Yield 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC=C(C#N)S(=O)(=O)Cc1ccc(C)cc1
Reaction #92044
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(CCSC(F)(F)F)S(=O)(=O)CCC(F)(F)C(F)(F)F
Reaction #167585
2-(3,3,4,4,4-Pentafluoro-butane-1-sulfonyl)-4-trifluoromethylsulfanyl-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(CCSC(F)(F)F)S(=O)(=O)Cc1ccc(Cl)nc1
Reaction #167588
2-(6-Chloro-pyridin-3-ylmethanesulfonyl)-4-trifluoromethylsulfanyl-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(CCSC(F)(F)F)S(=O)(=O)Cc1ccc(C(F)(F)F)nc1
Reaction #167589
2-(6-Trifluoromethyl-pyridin-3-ylmethanesulfonyl)-4-trifluoromethylsulfanyl-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(CCSC(F)(F)F)S(=O)(=O)CCSC(F)(F)F
Reaction #167592
2-Methyl-4-trifluoromethylsulfanyl-2-(2-trifluoromethylsulfanyl-ethanesulfonyl)-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C#N)S(=O)(=O)c1ccccc1
Reaction #173418
DOI: 10.1039/C8SC04228D
COc1ccc(C(C#N)(CC(C)CN2CCc3cc(OC)c(OC)cc3C2)Sc2ccc(C)cc2)cc1OC
Reaction #177996
DOI: 10.1039/C8SC04228D
CC(NC(Nc1cccc(C#N)c1)=C(C#N)S(=O)(=O)c1ccc(Cl)cc1)C(C)(C)C
Reaction #185696
DOI: 10.1039/C8SC04228D
CC(C)C(C)NC(Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1)=C(C#N)S(=O)(=O)c1ccc(Cl)cc1
Reaction #195438
DOI: 10.1039/C8SC04228D
CC1=C(C#N)S(=O)(=O)c2ccc(F)cc2N1
Reaction #196402
DOI: 10.1039/C8SC04228D
COc1cc(CC#N)c(C)cc1[N+](=O)[O-]
Reaction #197524
DOI: 10.1039/C8SC04228D
N#CC1=C(c2ccccc2)Nc2ccccc2S1=O
Reaction #197981
DOI: 10.1039/C8SC04228D
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