61715-75-1

Usage

Uses

Used in Pharmaceutical Industry:
1-N-Butyl-1-phenylhydrazine is used as a key intermediate in the synthesis of anti-inflammatory drugs, contributing to the development of medications that help alleviate inflammation and associated symptoms.
Used in Agrochemical Industry:
In the agrochemical sector, 1-N-Butyl-1-phenylhydrazine serves as an essential component in the production of pesticides, aiding in the creation of compounds that protect crops from pests and diseases, thereby ensuring agricultural productivity.

InChI:InChI=1/C10H16N2/c1-2-3-9-12(11)10-7-5-4-6-8-10/h4-8H,2-3,9,11H2,1H3

Upstream product

• 25413-69-8 N-butyl-N-nitroso-aniline 
• 542-69-8 1-iodo-butane 
• 27843-96-5 (1E)-1-(2-phenylhydrazin-1-ylidene)propan-2-one 
• 109-69-3 n-Butyl chloride 
• 100-63-0 phenylhydrazine 
• 3314-35-0 3-Amino-1-phenyl-2-pyrazoline 
• 106087-12-1 3-Amino-1-butyl-1-phenyl-4,5-dihydro-1H-pyrazol-1-ium; iodide 

Downstream Products

• 121965-76-2 D-arabino-[2]hexosulose-1-(butyl-phenyl-hydrazone)-2-phenylhydrazone 
• 1570062-09-7 1-butyl-2-butylidene-1-phenylhydrazine 
• 1914-00-7 1-butyl-3-methyl-1H-indole 
• 1570062-11-1 1-butyl-2-heptylidene-1-phenylhydrazine 
• 343777-43-5 C₁₃H₂₀N₂ 
• 1570062-21-3 3-benzyl-1-butyl-1H-indole 
• 342893-38-3 C₁₄H₂₂N₂ 
• 1570062-25-7 4-(1-butyl-1H-indol-3-yl)phenol 
• 1126-78-9 N-(n-butyl)aniline 
• 2834-92-6 1-amino-2-naphthol 
• 1415425-72-7 1-butyl-3-(4-chlorophenyl)-1H-indole 
• 110336-54-4 D-arabino-[2]hexosulose-1-(butyl-phenyl-hydrazone)-2-hydrazone 

Relevant academic research and scientific papers

SIMPLE PREPARATION OF N-ALKYL-N-ARYLHYDRAZINES FROM DIAZOTABLE N-ARYLAMINES

Phase-Transfer-catalyzed N-alkylation of arylhydrazones 2, followed by hydrazinolysis with hydrazine hydrate in the presence of concentrated hydrochloric acid, provides a new access to N-alkyl-N-arylhydrazines 3.

AMIDRAZONES 9. CONVENIENT SYNTHESIS OF 1-ALKYL-1-PHENYLHYDRAZINES AND α,β-UNSATURATED AMIDRAZONES VIA BASE-PROMOTED REACTIONS OF 1,1-DISUBSTITUTED-3-AMNIO-4,5-DIHYDRO-1H-PYRAZOLIUM SALTS.

A simple, efficient procedure for the conversion of phenylhydrazine to 1-alkyl-1-phenylhydrazines via base-promoted hydrolysis of 1-alkyl-3-amino-4,5-dihydro-1-phenyl-1H-pyrazolium iodides (2) is described.N',N'-disubstituted hydrazones of trans-cinnamamide and acrylamide are obtained by Hofmann-type ring openings of 1,1-disubstituted-3-amino-4,5-dihydro-5-phenyl (or 5-unsubstituted) -1H-pyrazolium halides (5,7).