phenylisothiocyanate

O=C(Nc1ccc(NC(=S)Nc2ccccc2)cc1)c1ccc(NC(=S)Nc2ccccc2)cc1
Reaction #850
colorless crystal
収率 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)Oc2ccc(C#N)cc2C(C(=S)Nc2ccccc2)=C1O
Reaction #64343
N-phenyl-6- cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
収率 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)/N=C1\SCC(=O)N1c1ccccc1
Reaction #66984
3-phenyl-2-[(Z)-isopropylimino]-thiazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(CC(=O)O)c1ccc(NC(=O)Cc2ccc3nc(Nc4ccccc4)oc3c2)cn1
Reaction #77977
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CC(Sc1ccccc1)=C1SCCN1c1ccccc1
Reaction #78235
title compound
収率 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CN1CCN(C)C1=NC(=S)Nc1ccccc1
Reaction #94840
N-(1,3-dimethyl-2-imidazolidinylidene)-N'-phenyl-thiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(Cn2c(=O)n(C)c(=O)c3c(Nc4ccccc4)n[nH]c32)cc1
Reaction #159872
product
収率 414.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)/N=C1\SCC(=O)N1c1ccccc1
Reaction #167182
3-phenyl-2-[(Z)-isopropylimino]-thiazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)Cn1c(=O)n(C)c(=O)c2c(Nc3ccccc3)[nH]nc21
Reaction #168589
product
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1CC=[SH]C1=NC(=S)Nc1ccccc1
Reaction #179821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)N(Cc1ccc(Cl)cc1)C(=S)Nc1ccccc1
Reaction #182449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CN(C(=S)Nc2ccccc2)Cc2sccc21
Reaction #187342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C(=S)Nc1ccccc1)C1CCN(CCc2c[nH]c3ccccc23)CC1
Reaction #190465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1c(=NC(=S)Nc2ccccc2)n(C)c2ccccc21
Reaction #191391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(c2c[nH]c3ccc(NC(=S)Nc4ccccc4)cc23)CC1
Reaction #192535
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCCNC(=S)Nc1ccccc1
Reaction #192959
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
S=C(Nc1ccccc1)Nc1ncccc1OCc1c(Cl)cccc1Cl
Reaction #193957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1cc(NC(=S)Nc2ccccc2)ccc1O
Reaction #197130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2OCCC1(CO)COC(=S)Nc1ccccc1
Reaction #201884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)Oc2ccc(C#N)cc2[C@@H](NC(=S)Nc2ccccc2)[C@@H]1O
Reaction #216360
title compound
収率 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
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