Substructure Search

8071

CCc1cc2nonc2c(NS(=O)(=O)c2cccc3c(N(C)C)cccc23)c1C#N
Reaction #1718
5-dimethylamino- N-(5-cyano-6-ethyl-2,1,3-benzoxadiazol-4-yl)-1-naphthalenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCc1ccc(-c2ccc(C#N)cc2)nc1
Reaction #4029
2-(p-cyanophenyl)-5-octylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(Br)cc(C#N)c21
Reaction #5024
compound
Yield 81.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Br)cc1Br
Reaction #7063
title compound
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(C#N)=C1c1ccc(OC)cc1C2
Reaction #7930
9a-butyl-4-cyano-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(C#N)=C1c1ccc(OC)c(Cl)c1C2
Reaction #7981
9a-butyl-8-chloro-4-cyano-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
Yield 73.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(C#N)c1C(=O)OC
Reaction #10044
product
Yield 69.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(C#N)nc3N21
Reaction #12018
desired compound
Yield 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1ccc2c(C#N)cc(C(=O)OC)cc21
Reaction #42458
title compound
Yield 47.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(C#N)cc(C(=O)OC)cc21
Reaction #42472
title compound
Yield 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)c1nccc2ccc(C#N)cc12
Reaction #42538
1-(dipropylamino)isoquinoline-7-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C#N)cc(C(=O)OC)c1
Reaction #42617
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)CNCc1ccc2cc[nH]c2c1
Reaction #42620
isoquinoline carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cccc(C(=O)OCC)c1
Reaction #43282
compound 7
Yield 68.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C=O)cc2c1OCC2
Reaction #43452
desired product
Yield 61.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CC(N)=O)ccc(C#N)c1Cl
Reaction #43461
nitrile
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C=O)cc2c1OCC2
Reaction #43640
desired product
Yield 61.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(F)(F)F)ccc1N
Reaction #45308
2-amino-5-(trifluoromethyl)benzonitrile
Yield 105.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(C#N)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#N)cc(C(F)(F)F)c1
Reaction #45342
3-methoxy-5-(trifluoromethyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
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