Substructure Search

OCc1ccc(Cl)cc1

CCC(=O)OC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CCC(=O)OC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1937
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccc(Cl)c(Cl)c2)CCNCC1
Reaction #5251
compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNCCC1(O)c1ccc(Cl)cc1
Reaction #42975
4-(4-Chloro-phenyl)-3,3-dimethyl-piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)Nc2cc(Cl)c(Cl)cc2C1(O)C(=O)NC(N)=S
Reaction #62823
6,7-dichloro-3-methyl-4-hydroxy-4-thioureidocarbonyl-2-oxo-1,2,3,4-tetrahydroquinazoline
Yield 33.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)Nc2cc(Cl)c(Cl)cc2C12NC(=O)NC2=O
Reaction #62824
6,7-dichloro-3-methyl-spiro[1,2,3,4-tetrahydroquinazoline-4,4'-imidazolidine]-2,2',5'-trione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC)c(Cl)c([N+](=O)[O-])c1
Reaction #91032
methyl 4-chloro-3-methoxy-5-nitrobenzoate
Yield 68.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(Cl)c(OC)c1
Reaction #91033
methyl 3-amino-4-chloro-5-methoxybenzoate
Yield 103.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #91063
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2CCCC2)c(C(F)(F)F)c1
Reaction #91064
title compound
Yield 95.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #91067
title compound
Yield 92.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(OCc1ccc(Cl)cc1)N1CCNCC1COc1cccnc1
Reaction #157376
desired product
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(O)c2ccc(Cl)c(Cl)c2)ccc1-c1cnc(C)o1
Reaction #158277
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(OCc2ccc(Cl)c(Cl)c2)c2ccc(F)c(F)c2)ccc1-c1cnc(C)o1
Reaction #158283
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc2[nH]nnc2c1)N1CCN(C(=O)OCc2ccc(Cl)cc2)CC1
Reaction #164813
4-chlorobenzyl 4-(2-1H-benzotriazol-5-ylacetyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OCCOC2CCCCO2)c(Oc2ccccc2OC)c([N+](=O)[O-])c1
Reaction #181053
DOI: 10.1039/C8SC04228D
CCOC(=O)N(C)c1c(C(=O)O)ccc(Cl)c1Cl
Reaction #195675
DOI: 10.1039/C8SC04228D
O=C1C2=C(CCCC2)C(=O)N1c1cccc(OCc2ccc(Cl)cc2)n1
Reaction #196466
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)OCCC2(c3ccc(Cl)c(Cl)c3)CN(C(=O)Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CCO2)cc1
Reaction #198209
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(Cl)cc2)C(OCc2ccc3ccccc3c2)C1
Reaction #199615
DOI: 10.1039/C8SC04228D
CN1C(=O)OC(C)(c2ccc(Cl)cc2)c2cc(Nc3ccc(Br)cc3)ccc21
Reaction #207648
DOI: 10.1039/C8SC04228D
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