Substructure Search

962684

S=C=Nc1ccc2c(c1)OCCO2
Reaction #5944
3,4-ethylenedioxyphenylisothiocyanate
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N=C=S)cc(OC)c1OC
Reaction #5952
3,4,5-trimethoxyphenylisothiocyanate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=S)OCCCN2CCN(c3cccc(Cl)c3)CC2)cc(OC)c1OC.Cl
Reaction #5953
title compound
Yield 38.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=S)OCCCN2CCN(c3ccccc3Cl)CC2)cc(OC)c1OC.Cl
Reaction #5954
title compound
Yield 42.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46423
powder
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46426
powder
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(C(C)C(=O)Oc3ccc(N=C=S)cc3)ccc2c1
Reaction #46913
4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(N=C=S)cc1
Reaction #46914
4-isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccccc1C(=O)Oc1ccc(N=C=S)cc1
Reaction #46915
4-isothiocyanatophenyl 2-acetoxybenzoate
Yield 7.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(N=C=S)ccc1Oc1cc(Cl)ccc1Cl
Reaction #62038
crude product
Yield 97.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(C(N)=O)C(=S)Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62039
crude product
Yield 82.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(C(C)C(=O)Oc3ccc(N=C=S)cc3)ccc2c1
Reaction #72447
4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(N=C=S)cc1
Reaction #72448
4-isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccccc1C(=O)Oc1ccc(N=C=S)cc1
Reaction #72449
4-isothiocyanatophenyl 2-acetoxybenzoate
Yield 7.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=S)NCc2ccc(-c3ncn(-c4ccc(OC(F)(F)C(F)(F)F)cc4)n3)cc2)c(C)c1
Reaction #90345
title compound
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc2c(c1)OCCO2
Reaction #182775
DOI: 10.1039/C8SC04228D
CC(=NNC(=S)Nc1ccc2c(c1)OCCO2)c1csc(-c2ccc(Cl)c(Cl)c2)c1O
Reaction #191712
DOI: 10.1039/C8SC04228D
COc1ccc(N=C=S)c(N2CCOCC2)c1
Reaction #201177
DOI: 10.1039/C8SC04228D
N#CC(C(N)=O)C(=S)Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #230723
DOI: 10.1039/C8SC04228D
CCC1(C)Oc2ccc(NC(=S)N(C)N)cc2O1
Reaction #233589
DOI: 10.1039/C8SC04228D
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