3-(1,3-benzodithiol-2-ylideneamino)-2-sulfanylidene-1,3-thiazolidin-4-one

O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #175164
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(=Cc2cccc(C(F)(F)F)c2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #280892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #406218
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #763407
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #778009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1C(=CCc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2421582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506323
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
CCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #2506324
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
CCCCCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #2506325
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
O=C1C(=CCc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506326
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
O=C1C(=Cc2cccc(C(F)(F)F)c2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506327
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506748
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
CCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #2506749
title compound
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
CCCCCCCC=C1SC(=S)N(N=c2sc3ccccc3s2)C1=O
Reaction #2506750
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
O=C1C(=CCc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506751
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08
O=C1C(=Cc2cccc(C(F)(F)F)c2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #2506752
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08