部分構造検索

9267

O=C1CCCN1C1CCCCC1
Reaction #4965
cyclohexyl pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)c1c(S(=O)(=O)O)c2[nH]c1cc1nc(cc3ccc(cc4nc(c2S(=O)(=O)O)C=C4)[nH]3)-c2ncccc2-1.[NH4+].[NH4+].[NH4+]
Reaction #214332
Tri sulfo pyrido porphine, tri ammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)c1c(S(=O)(=O)O)c2[nH]c1cc1nc(cc3ccc(cc4nc(c2S(=O)(=O)O)C=C4)[nH]3)-c2ncccc2-1.[NH4+].[NH4+].[NH4+]
Reaction #214670
Tri sulfo pyrido porphine, tri ammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1ncc2c1Nc1cc(Cl)ccc1N(C(=O)c1ccc(CN)c(F)c1)C2
Reaction #308143
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2c1Nc1cc(Cl)ccc1N(C(=O)c1ccc(CNC(=O)C3CC3)c(F)c1)C2
Reaction #308144
title compound
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)NCc1ccc(C(=O)N2Cc3cnn(C)c3Nc3cc(Cl)ccc32)cc1F
Reaction #308145
title compound
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)NCc1ccc(C(=O)N2Cc3cnn(C)c3Nc3cc(Cl)ccc32)cc1F
Reaction #308146
title compound
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)NCc1ccc(C(=O)N2Cc3cnn(C)c3Nc3cc(Cl)ccc32)cc1F
Reaction #308147
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2c1Nc1cc(Cl)ccc1N(C(=O)c1ccc(CNC(=O)CNC(=O)OC(C)(C)C)c(F)c1)C2
Reaction #308154
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(S(=O)(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)c1
Reaction #311520
8-m-nitrobenzenesulfonamido-1,3,6-naphthalenetrisulfonic acid
収率 80.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)ccc1S(=O)(=O)Nc1cc(S(=O)(=O)O)cc2cc(S(=O)(=O)O)cc(S(=O)(=O)O)c12
Reaction #311522
8-(5-amino-o-toluenesulfonamido)-1,3,6-naphthalenetrisulfonic acid
収率 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1C1CCCCC1
Reaction #334957
cyclohexyl pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc([N+](=O)[O-])ccc1S(=O)(=O)Nc1cc(S(=O)(=O)O)cc2cc(S(=O)(=O)O)cc(S(=O)(=O)O)c12
Reaction #350201
8-(5-nitro-o-toluenesulfonamido)-1,3,6-naphthalenetrisulfonic acid
収率 841.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=O)c2ccc([N+](=O)[O-])cc2S(=O)(=O)O)ccc1S(=O)(=O)Nc1cc(S(=O)(=O)O)cc2cc(S(=O)(=O)O)cc(S(=O)(=O)O)c12
Reaction #350202
8-[5-(4-nitro-2-sulfobenzamido)-o-toluenesulfonamido]-1,3,6-naphthalenetrisulfonic acid
収率 166.9%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(S(=O)(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)c1
Reaction #350203
8-m-nitrobenzenesulfonamido-1,3,6-naphthalenetrisulfonic acid
収率 80.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(S(=O)(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)c1
Reaction #350241
8-m-nitrobenzenesulfonamido-1,3,6-naphthalenetrisulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)ccc1S(=O)(=O)Nc1cc(S(=O)(=O)O)cc2cc(S(=O)(=O)O)cc(S(=O)(=O)O)c12
Reaction #350243
8-(5-amino-o-toluenesulfonamido)-1,3,6-naphthalenetrisulfonic acid
収率 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)c1cc(N=C=S)c2c(S(=O)(=O)O)cc(S(=O)(=O)O)cc2c1
Reaction #368061
8-isothiocyanato-1,3,6-naphthalenetrisulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #517781
solid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=c2ccccc2=N1
Reaction #567079
Benzimidazolone
DOI: 10.6084/m9.figshare.5104873.v1
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