子结构搜索

7086

CC(C)NCCSc1ccc(Cl)cc1.Cl
Reaction #4283
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCSc1ccc(Cl)c(Cl)c1.Cl
Reaction #4288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #4291
white crystalline product
收率 32.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #4296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(S(=O)(=O)CCNC(C)C)cc1.Cl
Reaction #4308
N-[2-[(4-Ethoxyphenyl)sulfonyl]ethyl]-2-propanamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(O)cc1.Cl
Reaction #4309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5cc(Cl)c(Cl)cc5Cl)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #188091
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccc(Cl)c(Cl)c5)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #300622
DOI: 10.1039/C8SC04228D
CCOc1ccc(S(=O)(=O)CCNC(C)C)cc1.Cl
Reaction #417585
N-[2-[(4-Ethoxyphenyl)sulfonyl]ethyl]-2-propanamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(OCCN(C)C)cc1.O=C(O)/C=C\C(=O)O
Reaction #417590
product
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(C2=C(C(=O)OC(c3ccccc3)c3ccccc3)N3C(=O)C(NC(=O)CSc4ccc(Cl)c(Cl)c4)C3SC2)s1
Reaction #457785
3-(2-aminothiazol-5-yl)-2-benzhydryloxycarbonyl-7-(3,4-dichlorophenylthio)acetamido-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCSc1ccc(Cl)cc1.Cl
Reaction #832336
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCSc1ccc(Cl)c(Cl)c1.Cl
Reaction #832341
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #832344
white crystaline product
收率 32.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #832350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(S(=O)(=O)CCNC(C)C)cc1.Cl
Reaction #832362
N-[2-[(4-Ethoxyphenyl)sulfonyl]ethyl]-2-propanamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(O)cc1.Cl
Reaction #832363
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Sc2ccc(Cl)cc2Cl)CCN1C1CCCCC1
Reaction #900495
DOI: 10.1039/C8SC04228D
CCC[C@H](NC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccc(Cl)cc2Cl)CN1C(=O)C1(c2ccc(Cl)cc2)CC1)C(=O)C(=O)NC1CC1
Reaction #1112525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(Sc2ccc(Cl)cc2Cl)CC1C(=O)NC1(C#N)CC1
Reaction #1212751
DOI: 10.1039/C8SC04228D
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