Substructure Search

CN(C)N.Cl.Cl

O=C(Nc1ccc(Oc2ccc(Cl)cc2)cc1)N1CC(c2ccccc2)=C(c2ccc(Cl)cc2)N1
Reaction #63967
3-(4-chlorophenyl)-N-[4-(4-chlorophenoxy)phenyl]-4-phenylpyrazoline-1-carboxamide
Yield 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)N1C(=O)c2ccccc2C1=O
Reaction #72711
desired product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2c(Cl)cccc2Cl)cc1OC
Reaction #87539
desired product
Yield 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(Cl)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87540
desired product
Yield 103.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=O)NC(=O)N(NC(=O)OC(C)(C)C)c2c(Cl)cccc2Cl)cc1OC
Reaction #87597
desired product
Yield 81.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2nn(-c3c(Cl)cccc3Cl)c(=O)[nH]2)cc1OC
Reaction #87598
desired product
Yield 52.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Nc1cc(Cl)c(Cl)cc1[N+](=O)[O-]
Reaction #174287
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(Oc2ncc(Cl)cc2Cl)cc1)C(=O)NOCC(=O)NN1CCCCC1
Reaction #183216
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(C(F)(F)F)cc1)N1CC(c2ccc(Cl)cc2)C(c2ccc(Cl)cc2)N1
Reaction #187459
DOI: 10.1039/C8SC04228D
COc1c(C(=O)NN2CCOCC2)nn(-c2ccccc2Cl)c1-c1ccc(Cl)cc1
Reaction #189552
DOI: 10.1039/C8SC04228D
CC(C)N1C(c2ccncc2)C(c2ccc(Cl)c(Cl)c2)C(=O)N1C
Reaction #192219
DOI: 10.1039/C8SC04228D
CC1=NN(c2ccccc2)C(=O)C1C(=O)Nc1ccc(Cl)c(Cl)c1
Reaction #192547
DOI: 10.1039/C8SC04228D
CC(NC(=O)c1cc(Cl)ccc1NC(=O)C1CC(Br)=NN1c1ncccc1Cl)C1CC1
Reaction #194377
DOI: 10.1039/C8SC04228D
C=CCCC(OC)C(C)C(=O)NC(C(=O)NC(Cc1cccc(O[Si](C)(C)C(C)(C)C)c1)C(=O)N1CCCC(C(=O)O)N1)C(C)C
Reaction #199730
DOI: 10.1039/C8SC04228D
CC(NC(=O)c1cc(Cl)ccc1NC(=O)C1CC(Br)=NN1c1ncccc1Cl)C1CC1
Reaction #200538
DOI: 10.1039/C8SC04228D
CC1=NN(c2ccc(Cl)c(Cl)c2)C(=O)C1C(=O)Nc1ccc(Cl)c(Cl)c1
Reaction #203449
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1nc2cc(Cl)c(Cl)cc2nc1N(N)C(=O)Nc1ccccc1
Reaction #204646
DOI: 10.1039/C8SC04228D
CC1CN(C)N(c2cc(Cl)cc(Cl)c2)C(=O)N1
Reaction #204703
DOI: 10.1039/C8SC04228D
Cc1nn2c(-c3ccc(Cl)cc3Cl)c(C)oc2c1N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #213799
DOI: 10.1039/C8SC04228D
NC(=O)NN(C(=O)C=C(Cl)Cl)c1ccccc1
Reaction #214901
1-(β,β-dichloroacryloyl)-1-phenyl-semicarbazide
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
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