67156-57-4

Usage

Uses

Used in Pharmaceutical Research and Development:
1-(2-Brom-4-Methylphenyl)hydrazine, HCl is used as a research chemical for the synthesis of organic molecules and in medicinal chemistry to develop new drugs and treatments. Its unique structure with a bromine and methyl group on a phenyl ring, along with the increased solubility and stability provided by the HCl salt, make it a valuable compound for exploring novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-Brom-4-Methylphenyl)hydrazine, HCl is utilized as a building block or intermediate in the creation of complex organic molecules. Its reactivity and functional groups allow for various chemical reactions, facilitating the development of new compounds with potential applications in different industries.
Used in Medicinal Chemistry:
1-(2-Brom-4-Methylphenyl)hydrazine, HCl is employed in medicinal chemistry as a key component in the design and synthesis of new pharmaceuticals. Its structural features can be leveraged to create molecules with specific biological activities, targeting various diseases and conditions. 1-(2-BroMo-4-Methylphenyl)hydrazine, HCl's potential in drug discovery makes it an important tool for researchers in the pharmaceutical industry.

InChI:InChI=1/C7H9BrN2/c1-5-2-3-7(10-9)6(8)4-5/h2-4,10H,9H2,1H3

Upstream product

• 583-68-6 2-bromo-p-toluidine 
• 539-44-6 N-4-methylphenylhydrazine 
• 7647-01-0 hydrogenchloride 
• 7726-95-6 bromine 
• 409321-38-6 2-bromo-4-methyl-N-nitro-aniline 

Downstream Products

• 33720-87-5 benzoic acid-[N'-(2-bromo-4-methyl-phenyl)-hydrazide] 
• 591-17-3 meta-bromotoluene 
• 1338369-90-6 N-tert-butoxycarbonyl-N'-(2-bromo-4-methylphenyl)hydrazine 
• 1338369-61-1 N-tert-butoxycarbonyl-N'-(2-bromo-4-methylphenyl)diazene 
• 1338369-70-2 N-tert-butoxycarbonyl-N'-(2-bromo-4-methylphenyl)-N'-(pyridin-3-yl)hydrazine 
• 1338369-72-4 N-tert-butoxycarbonyl-N'-(2-bromo-4-methylphenyl)-N'-butylhydrazine 
• 1338369-81-5 N-(2-bromo-4-methylphenyl)-N-(pyridin-3-yl)hydrazine 
• 1338369-83-7 N-butyl-N-(2-bromo-4-methylphenyl)hydrazine 
• 1338369-77-9 N-(pyridin-3-yl)-2-bromo-4-methylaniline 
• 1019542-99-4 N-butyl-2-bromo-4-methylaniline 
• 1331944-35-4 C₂₂H₂₁FN₂ 
• 1331947-87-5 6-bromo-5-(2-(4-fluorophenyl)allyl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole 

Relevant academic research and scientific papers

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.