Substructure Search

940

CN(C)[C@H]1CCN(c2cc(Cl)ccc2C#N)C1
Reaction #177
Yield 69.3%
N#Cc1ccc(Cl)cc1N1CCNCC1
Reaction #413
Yield 0.0%
N#Cc1ccc(Cl)cc1Nc1cccc(Cl)n1
Reaction #519
Yield 93.5%
N#Cc1ccc(Cl)cc1Cl
Reaction #56370
2,4-dichlorobenzonitrile
Yield 79.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)c(N)cc1Cl
Reaction #76125
solid
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)c(N)cc1Cl
Reaction #76126
2-Amino-4-chloro-5-methylbenzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1Nc1cc(Cl)ncc1Cl
Reaction #90808
4-chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile
Yield 57.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc(Nc3cc(Cl)ccc3C(=O)O)c(Cl)cn2)n(C(C)C)n1
Reaction #90809
4-Chloro-2-[(5-chloro-2-{[3-methyl-1-(1-methylethyl)-1H-pyrazol-5-yl]amino}-4-pyridinyl)amino]benzoic acid
Yield 6.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(C#N)c([N+](=O)[O-])c2)C[C@H](C)N1
Reaction #217597
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccccc2)cc1NC(=O)c1cc(N2CCCCC2)ccc1OCc1ccccc1
Reaction #229508
DOI: 10.1039/C8SC04228D
CCN1C(C)(C)CC(Nc2cc(Cl)ccc2C#N)CC1(C)C
Reaction #268494
DOI: 10.1039/C8SC04228D
N#Cc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #275118
DOI: 10.1039/C8SC04228D
Cc1cc(C#N)c(NC2CCCCC2NC(=O)OC(C)(C)C)cc1Cl
Reaction #290738
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCC1Nc1cc(Cl)c(Cl)cc1C#N
Reaction #292561
DOI: 10.1039/C8SC04228D
COC(=O)c1sc2cc(Cl)ccc2c1N
Reaction #322247
title compound
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(Cl)cc1N
Reaction #331395
title material
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2ccccc2)nc2cc(Cl)ccc12
Reaction #331400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1NC(=O)c1ccccc1
Reaction #331401
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1NC(=O)c1cc(N2CCCCC2)ccc1OCc1ccccc1
Reaction #368185
DOI: 10.1039/C8SC04228D
N#Cc1ccc(Cl)cc1NC(CCI)c1ccccc1
Reaction #369369
DOI: 10.1039/C8SC04228D
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