This compound is a mixture of related cyanoacrylamide derivatives featuring a benzothiophene moiety, each substituted with various aryl groups including bromo, chloro, methoxy-dimethyl, methyl, and nitro functionalities. The structure contains an amide, nitrile, and ether group, along with aromatic and heterocyclic rings, indicating potential utility in pharmaceutical research.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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2-(4'-Chloro-[1,1'-biphenyl]-4-yl)benzo[d]oxazole
chemical intermediate
3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Research reagent
1H-indazole
research compound
1,7-diazaindene
research compound
3-(3-bromophenyl)-2-cyano-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)prop-2-enamide;3-(2-chlorophenyl)-2-cyano-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)prop-2-enamide;2-cyano-3-(3-methoxy-4,5-dimethylphenyl)-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)prop-2-enamide;2-cyano-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)-3-(3-methylphenyl)prop-2-enamide;2-cyano-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)-3-(2-nitrophenyl)prop-2-enamide;2-cyano-N-(1-methylidene-1-oxo-1-benzothiophen-6-yl)-3-(4-nitrophenyl)prop-2-enamide
XYDYYXUYLOJNII-UHFFFAOYSA-N
CC1=CC(=CC=C1)C=C(C#N)C(=O)NC2=CC3=C(C=C2)C=CS3(=C)=O.CC1=CC(=CC(=C1C)OC)C=C(C#N)C(=O)NC2=CC3=C(C=C2)C=CS3(=C)=O.C=S1(=O)C=CC2=C1C=C(C=C2)NC(=O)C(=CC3=CC=C(C=C3)[N+](=O)[O-])C#N.C=S1(=O)C=CC2=C1C=C(C=C2)NC(=O)C(=CC3=CC(=CC=C3)Br)C#N.C=S1(=O)C=CC2=C1C=C(C=C2)NC(=O)C(=CC3=CC=CC=C3[N+](=O)[O-])C#N.C=S1(=O)C=CC2=C1C=C(C=C2)NC(=O)C(=CC3=CC=CC=C3Cl)C#N
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