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Usage

Uses

Used in Organic Synthesis:
Benzonitrile, 2-bromo-4-hydrazinylis used as a key intermediate in organic synthesis for the production of various other compounds. Its hydrazinyl group allows for the formation of different chemical structures, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In pharmaceutical research, Benzonitrile, 2-bromo-4-hydrazinylis utilized as a starting material for the development of new drugs. Its unique structure and functional groups enable the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in the Treatment of Certain Diseases and Disorders:
Benzonitrile, 2-bromo-4-hydrazinylhas been studied for its potential as a therapeutic agent in the treatment of certain diseases and disorders. Its hydrazinyl group may contribute to its biological activity, making it a promising candidate for further research and development in the pharmaceutical industry.
Used in Environmental and Health Risk Management:
Due to its potential risks to health and the environment, Benzonitrile, 2-bromo-4-hydrazinylis also used in the development of strategies for managing and mitigating these risks. This includes the design of safe handling procedures, waste disposal methods, and risk assessment studies to ensure the responsible use of this chemical compound in various applications.

Upstream product

• 57381-49-4 2-bromo-4-chloro-benzonitrile 
• 36282-26-5 2-bromo-4-fluorobenzonitrile 
• 131002-01-2 2-bromo-4-chlorobenzamide 

Downstream Products

• 908111-29-5 2-bromo-4-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)benzonitrile 
• 1008520-10-2 4-(3,6-Dimethyl-4-oxo-4H-pyrano[2,3-c]pyrazol-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide 
• 1008520-08-8 4-(3,6-Dimethyl-4-oxo-4H-pyrano[2,3-c]pyrazol-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzonitrile 
• 1008520-72-6 2-Bromo-4-[5-hydroxy-3-methyl-4-(3-methyl-but-2-enoyl)-pyrazol-1-yl]-benzonitrile 
• 1008520-04-4 2-Bromo-4-(3,6,6-trimethyl-4-oxo-5,6-dihydro-4H-pyrano[2,3-c]pyrazol-1-yl)-benzonitrile 
• 1008520-06-6 2-Bromo-4-(3,6-dimethyl-4-oxo-4H-pyrano[2,3-c]pyrazol-1-yl)-benzonitrile 
• 1246307-32-3 2-bromo-4-{N'-[2,2,2-trifluoro-1-(2-hydroxy-6-oxocyclohex-1-enyl)ethylidene]hydrazino}benzonitrile 

Relevant academic research and scientific papers

ANTIMICROBIAL COMPOSITIONS, METHODS OF USE, AND METHODS OF TREATMENT OF INFECTIONS

The present disclosure provides compositions including a compound (e.g., compounds A-D), pharmaceutical compositions including the compound, methods of treatment of a condition (e.g., an infection) or disease, methods of treatment using compositions or pharmaceutical compositions, and the like.

OMEGA-AMINO ACID DERIVATIVES OF BENZENE, PYRIDINE, AND PYRIDAZINE COMPOUNDS

Disclosed are compounds and pharmaceutically acceptable salts of Formula I wherein R1, R2, R3, R4, R5, R6, R7, n, Q1, Q2, Q3, Y, and X1/sub

Discovery of novel 2-aminobenzamide inhibitors of heat shock protein 90 as potent, selective and orally active antitumor agents

A novel class of heat shock protein 90 (Hsp90) inhibitors was developed from an unbiased screen to identify protein targets for a diverse compound library. These indol-4-one and indazol-4-one derived 2-aminobenzamides showed strong binding affinity to Hsp

Benzene, Pyridine, and Pyridazine Derivatives

Disclosed are compounds and pharmaceutically acceptable salts of Formula I wherein A, Q1, Q2, Q3, R31, and R41 are as defined herein. Compounds of Formula I are useful in the treatment of diseases and

Cyclohexylamino Benzene, Pyridine, and Pyridazine Derivatives

Disclosed are compounds and pharmaceutically acceptable salts of Formula (I), wherein Q1, Q2, RN, R1, R2, R5, R6, R7, R8, X1, X2, Xsu

TETRAHYDROINDOLONE AND TETRAHYDROINDAZOLONE DERIVATIVES

Disclosed are compounds and pharmaceutically acceptable salts of Formula (I): wherein R1, R2, R3, R4, R5, R6, R7, n, Q1, Q2, Q3, Y, and X1-X4 are as defined

Simplified Synthesis of the Precursor for the Azo Dye Chlorindazone DS

Recently, Chlorindazone DS 1 has become an important analytical reagent for the detection of gunshot residues from newly introduced ammunition. A simplified synthesis of the precursor of the azo dye 1, 3-amino-6-chloroindazole (2), from commercially available 2,4-dichlorobenzonitrile (3a) has been described. The physical and spectroscopical properties of the known compounds 1 and 2 have been completed. 2-Chloro-4-hydrazinobenzonitrile (4a), 2-bromo-4-hydrazinobenzonitrile (4b) and a new azo dye, 1-(3′-chloro-4′-cyanobenzene-1′-ylazo)-2-hydroxynaphthalene-3, 6-disulfonic acid, disodium salt (5), have been investigated.