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Organic compounds that consist of a benzene ring substituted with amino and carboxyl groups. Includes compounds that are derived from aminobenzoic acids.
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2-Amino-5-chlorobenzophenone is a substituted benzophenone that finds utility in various chemical syntheses. It is particularly noted for its role as a precursor in the synthesis of benzodiazepines, a class of psychoactive drugs. Derivatives of 2-Amino-5-chlorobenzophenone have also been observed to exhibit skeletal muscle relaxation activity.
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2-Amino-5-chlorobenzophenone is a substituted benzophenone that can be utilized in the synthesis of benzodiazepines. Derivatives of 2-Amino-5-chlorobenzophenone have demonstrated skeletal muscle relaxation activity.
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2-Amino-5-chlorobenzophenone is a substituted benzophenone and can be used in the synthesis of benzodiazepines. The derivative has skeletal muscle relaxation activity. It is a solid that appears light yellow to yellow in color.
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2-Amino-5-chlorobenzophenone is a substituted benzophenone that finds application in the synthesis of benzodiazepines. This derivative also exhibits skeletal muscle relaxation activity. It is intended for research use only and is not sold to patients.
Used in the synthesis of benzodiazepines.
Exhibits skeletal muscle relaxation activity.
Intended for research use only.
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Methanone, (2-amino-5-chlorophenyl)phenyl- is a high-purity substituted benzophenone (99.98%). It is primarily used in the synthesis of benzodiazepines. Derivatives of this compound have shown skeletal muscle relaxation activity and it is intended for research use only.