109221-88-7

Usage

Uses

Used in Organic Synthesis:
BIPHENYL-3-YL-HYDRAZINE HYDROCHLORIDE is used as a reagent for the preparation of various compounds in organic synthesis. Its versatility and stability make it a convenient choice for laboratory experiments and industrial processes.
Used in Medicinal Chemistry Research:
BIPHENYL-3-YL-HYDRAZINE HYDROCHLORIDE is used as a subject of interest in medicinal chemistry research due to its potential biological activities, including anti-inflammatory and anti-tumor properties. Its potential therapeutic uses are being explored for the development of new drugs and treatments.
Used in Pharmaceutical Industry:
BIPHENYL-3-YL-HYDRAZINE HYDROCHLORIDE is used as a chemical intermediate in the synthesis of pharmaceutical compounds. Its potential biological activities and ease of handling make it a valuable component in the development of new drugs and therapeutic agents.
Used in Chemical Research and Development:
BIPHENYL-3-YL-HYDRAZINE HYDROCHLORIDE is used as a research compound in the development of new chemical processes and technologies. Its unique properties and potential applications make it a valuable tool for scientists and researchers in various fields.

Upstream product

• 2243-47-2 3-biphenyl amine 
• 2113-58-8 3-nitro-1,1'-biphenyl 
• 2113-57-7 3-bromobiphenyl 

Downstream Products

• 180003-61-6 6-phenyl-2,3,3-trimethylindolenine 
• 920301-52-6 9-(phenyl)-2-hydroxy-5,11-dihydro-6H-benzo[a]carbazole-3-carboxylic acid 
• 1082241-77-7 C₂₃H₁₇NO₃ 

Relevant academic research and scientific papers

Synthesis of Aryl Hydrazines via CuI/BMPO Catalyzed Cross-Coupling of Aryl Halides with Hydrazine Hydrate in Water

The N,N’-bis(2,6-dimethylphenyl)oxalamide was discovered as a powerful ligand for Cu-catalyzed cross-coupling of aryl halides with hydrazine hydrate, leading to the formation of a variety of aryl hydrazines at 80 oC in water under the assistance of K3PO4 and 4 mol% cetyltrimethylammonium bromide from aryl bromides and aryl iodides. Good to excellent yields were observed in most cases.

Synthesis method of substituted phenylhydrazine and salt thereof

The invention relates to a novel synthesis method of substituted phenylhydrazine and salt thereof. A substituted phenyl diazene compound is reduced to generate the substituted phenylhydrazine; a reducing agent B is selected from one or several of a catalytic hydrogenating system, formic acid, formate and formic acid ester compound; the obtained substituted phenylhydrazine can be further acidified to prepare the substituted phenylhydrazine salt which is easily stored and transported. The synthesis method has the advantages that the yield rate is high, the cost is low, the reaction time is short, the technology operation and post-treatment are simple, and the amount of waste water, waste gas and waste residue is fewer; the component of the produced waste water is single, the recycling is convenient, the treatment cost is low, and the green chemical requirement is met; the synthesis method of the substituted phenylhydrazine is more suitable for the large-scale industrialized production.

Lipophilic cyanine dyes with enchanced aqueous solubilty

The present invention relates to a family of cyanine dyes possessing lipophilic alkyl chains and either one or more reactive functional groups, bromo or chloro, or phenyl, sulfophenyl or polysulfophenyl substituents or combinations thereof. The dyes of th

Lipophilic sulfophenylcarbocyanine dyes: Synthesis of a new class of fluorescent cell membrane probes

Two lipophilic sulfophenylcarbocyanine dyes, 3 and 4, were synthesized as a new class of fluorescent cell membrane probes. Compared with other commonly used membrane probes, the new dyes have improved fluorescent quantum yield, retention in cell membranes and are easier to use in staining cells.