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40566

C=CCN(CC(=O)c1ccns1)C(=O)OC(C)(C)C
Reaction #425260
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(CC(=O)c1ccns1)C(=O)OC(C)(C)C
Reaction #557388
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccc(Cl)cc1)(c1ccc(Cl)cc1)c1ccns1
Reaction #725375
α,α-Bis(4-chlorophenyl)-5-isothiazolemethanol
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1snc(Cl)c1Cl
Reaction #751909
DOI: 10.1039/C8SC04228D
OC1(c2ccns2)CCC2(CC1)OCCO2
Reaction #899020
DOI: 10.1039/C8SC04228D
OC(c1ccc(Cl)cc1)(c1ccc(Cl)cc1)c1ccns1
Reaction #1022122
DOI: 10.1039/C8SC04228D
C=CCN(CC(=O)c1ccns1)C(=O)OC(C)(C)C
Reaction #1706163
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=N[N+](=O)[O-])NCCSCc1ccsn1
Reaction #1921805
N-[2-(3-isothiazolylmethylthio)ethyl]-N'-methyl-N"-nitroguanidine
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccns2)CCC2(CC1)OCCO2
Reaction #2183402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccns1
Reaction #2260197
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cn1cc(C(=O)c2ccn3c2CSC3c2cccnc2)c2ccc(-c3ccc(F)cc3)cc21
Reaction #2297792
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1snc(Cl)c1Cl
Reaction #2342671
3,4-dichloro-5-isothiazolecarboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1