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Cc1nc2cc(N)ccc2s1.Cl.Cl

Cc1nc2cc(NC(=O)Oc3ccc([N+](=O)[O-])cc3)ccc2s1.Cl
Reaction #157338
4-nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)c3cc(Cl)ccc3Cl)ccc2s1
Reaction #179426
DOI: 10.1039/C8SC04228D
Cc1nc2cc(Br)ccc2s1
Reaction #489281
2-methyl-5-bromobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(NC(=O)c3ccc(-c4ccc(F)cc4)nc3C)ccc2s1
Reaction #578752
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(NC(=O)Oc3ccc([N+](=O)[O-])cc3)ccc2s1.Cl
Reaction #636875
4-nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Br)ccc2s1
Reaction #970769
2-methyl-5-bromobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)c3cc(Cl)cc(Cl)c3)ccc2s1
Reaction #1019536
DOI: 10.1039/C8SC04228D
Cc1nc2cc(NC(=O)Oc3ccc([N+](=O)[O-])cc3)ccc2s1.Cl
Reaction #1574914
4-nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Br)ccc2s1
Reaction #1604196
2-methyl-5-bromobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Br)ccc2s1
Reaction #1613895
2-methyl-5-bromobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)c3cc(Cl)cc(Cl)c3)ccc2s1
Reaction #1853505
3,5-Dichloro-N-(4-chloro-2-methyl-benzothiazol-5-yl)-benzamide
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)c3cc(Cl)ccc3Cl)ccc2s1
Reaction #1853508
2,5-dichloro-N-(4-chloro-2-methyl-benzothiazol-5-yl)-benzamide
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)Cc3ccc(Cl)cc3)ccc2s1
Reaction #1853513
N-(4-chloro-2-methyl-benzothiazol-5-yl)-2-(4-chloro-phenyl)-acetamide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)Cc3ccc(Cl)cc3Cl)ccc2s1
Reaction #1853514
N-(4-chloro-2-methyl-benzothiazol-5-yl)-2-(2,4-dichloro-phenyl)-acetamide
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Br)ccc2s1
Reaction #2071065
2-methyl-5-bromobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)Cc3ccc(Cl)cc3Cl)ccc2s1
Reaction #2238012
DOI: 10.1039/C8SC04228D
Cc1nc2cc(NC(=N)N)ccc2s1.O=[N+]([O-])O
Reaction #2376664
title compound
Ausbeute 47.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(Cl)c(NC(=O)Cc3ccc(Cl)cc3)ccc2s1
Reaction #2426439
DOI: 10.1039/C8SC04228D