Substructure Search

9899

CCOC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #5406
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methyl-thiazoline
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #5410
2-(N-ethylcarbamoylimino)-3-(3-trifluoromethylphenyl)-5-methylthiazoline
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=NC(=O)OCC)S1
Reaction #5414
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
Yield 44.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #5416
2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #50303
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl) 5-methylthiazoline
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #50306
2-(N-ethylcarbamoylimino)-3-(3-trifluoromethylphenyl)-5-methylthiazoline
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=NC(=O)OCC)S1
Reaction #50310
2-ethoxycarbonylimino-3-(3-trifluoromethyl-phenyl)-5-methylenethiazolidine
Yield 44.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #50312
2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #352912
2-imino-3-(3-(trifluoromethyl)phenyl)-5-methylidenethiazolidine
Yield 74.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=NC(=O)OCC)S1
Reaction #912179
DOI: 10.1039/C8SC04228D
CCOC(=O)N=C1[SH]=C(C)CN1c1cccc(C(F)(F)F)c1
Reaction #1323622
DOI: 10.1039/C8SC04228D
CCOC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #1808219
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylthiazoline
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N=c1sc(C)cn1-c1cccc(C(F)(F)F)c1
Reaction #1808223
2-(N-ethylcarbamoylimino)-3-(3-trifluoromethylphenyl)-5-methylthiazoline
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=NC(=O)OCC)S1
Reaction #1808227
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
Yield 44.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #1808229
2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #2226119
DOI: 10.1039/C8SC04228D
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #2246020
DOI: 10.1039/C8SC04228D
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #2298445
2-imino-3-(3-(trifluoromethyl)phenyl)-5-methylidenethiazolidine
Yield 74.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(c2cccc(C(F)(F)F)c2)C(=N)S1
Reaction #2380053
2-imino-3-(3-(trifluoromethyl)phenyl)-5-methylidenethiazolidine
Yield 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N=C1[SH]=C(C)CN1c1cccc(C(F)(F)F)c1
Reaction #2427504
DOI: 10.1039/C8SC04228D