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CCC(=O)c1ccc(Cl)cc1

O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #1587
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)C(=O)c1ccc(Cl)c([N+](=O)[O-])c1
Reaction #1590
4-chloro-3-nitrobenzoylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #1655
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #1680
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2160
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2185
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)c1ccc(Cl)cc1)n1ncn(-c2ccc(N3CCNCC3)nc2)c1=O.Cl
Reaction #2188
(±)-2-[1-(4-chlorobenzoyl)propyl]-2,4-dihydro-4-[6-(1-piperazinyl)-3-pyridinyl]-3H-1,2,4-triazol-3-one monohydrochloride
Выход 39.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2201
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2226
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(c2ccc(Cl)cc2)=NN1
Reaction #2261
6-(4-chlorophenyl)-4,5-dihydropyridazinone
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)C(=O)c1ccc(Cl)c([N+](=O)[O-])c1
Reaction #2263
4-chloro-3-nitrobenzoylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2284
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC=C(C(=O)OCC)C(=O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
Reaction #4361
Ethyl 2-(2,4-dichloro-5-fluoro-3-nitro-benzoyl)-3-ethoxyacrylate
DOI: 10.6084/m9.figshare.5104873.v1
OCCCC1=NN(c2nc3ccccc3s2)C(O)(c2ccc(Cl)cc2)C1
Reaction #5109
title compound ( 1 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-n3nc(CCCO)cc3-c3ccc(Cl)cc3)sc2c1
Reaction #5110
title compound 6
Выход 80.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC(=O)c1ccc(Cl)cc1.Cl
Reaction #40770
product
Выход 112.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2=NNCC2)cc1
Reaction #40771
yellow solid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC(=O)c1ccc(Cl)cc1
Reaction #50767
methyl 3-(4-chlorobenzoyl)propionate
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ncc[nH]1)c1ccc(Cl)cc1Cl
Reaction #60030
1-(2,4-dichlorophenyl)-2-imidazolylethan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ncc[nH]1)c1ccc(Cl)cc1Cl
Reaction #60087
1-(2,4-dichlorophenyl)-2-imidazolylethan-1-one
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
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