14722-38-4

Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
4-methylcinnoline is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structural properties make it a valuable building block in organic chemistry, contributing to the development of new and effective compounds for medical and agricultural applications.
Used in Organic Chemistry:
As a versatile building block, 4-methylcinnoline is employed in organic chemistry for the synthesis of complex organic molecules. Its presence in various chemical reactions allows for the creation of a wide range of compounds with diverse applications.
Used in Organic Electronics and Optoelectronic Devices:
4-methylcinnoline's unique structural properties also make it a promising candidate for use in the field of organic electronics and optoelectronic devices. Its potential applications in these areas include the development of organic light-emitting diodes (OLEDs), organic solar cells, and other electronic components that leverage the compound's electronic and optical properties.
Used in Biological Activities and Pharmacological Research:
4-methylcinnoline is being studied for its potential biological activities and pharmacological properties. Researchers are exploring its possible applications in medicine, such as its effects on various biological pathways and its potential as a therapeutic agent for specific conditions. This ongoing research aims to unlock the full potential of 4-methylcinnoline in the field of healthcare.

InChI:InChI=1/C9H8N2/c1-7-6-10-11-9-5-3-2-4-8(7)9/h2-6H,1H3

Upstream product

• 18592-02-4 cinnolin-4-yl-cyano-acetic acid ethyl ester 
• 89770-40-1 7-chloro-4-methyl-cinnoline 
• 64-17-5 ethanol 
• 7647-01-0 hydrogenchloride 
• 52562-19-3 2-isopropenylaniline 
• 7664-93-9 sulfuric acid 
• 551-93-9 2-aminoacetophenone 

Downstream Products

• 80334-73-2 4-(trichloromethyl)cinnoline 
• 21905-86-2 cinnoline-4-carboxylic acid 
• 83-34-1 3-Methylindole 
• 411210-76-9 o-Amino-β-methyl-phenaethylamin 
• 5387-96-2 4-<2-Furyl-(2)-vinyl>-cinnolin 
• 6334-39-0 4-trans-styryl-cinnoline 
• 77669-15-9 4-(3,4-dimethoxystyryl)cinnoline 

Relevant academic research and scientific papers

Flash vacuum pyrolysis of 1-azolyl-1-phenylhydrazono-2-propanones

(Chemical Equation Presented) Flash vacuum pyrolysis (FVP) of 1-(2-arylhydrazono)-1-(1H-1,2,4-triazol-1-yl)acetone 8a-c at 650°C and 2.67 Pa yielded 5-substituted 1-(1H-indazol-3-yl)ethanone 14a-c and 4,6-disubstituted cinnoline 18a-c. Similarly FVP of 1-(1H-benzo[d]imidazol-1-yl)-1-(2- phenylhydrazono)acetone 9a-c gave 8H-benzo[4′,5′]imidazo[2′, 1′:5,1]pyrrolo[2,3-c]cinnoline derivatives 23a-c. A plausible mechanism is suggested to account for their transformation based on the kinetics and products of reaction.

Tert -Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied

A green method to synthesize cinnolines by 6π electrocyclic reaction with alkenyl amines and TBN has been developed. TBN plays a dual role both as a nitrogen atom source and an oxidant in this procedure. Relevant mechanism experiments reveal that the reaction proceeds through electrocyclic reaction and with diazo hydroxide as a key intermediate.

Use of certain cinnoline-4-carboxylic acids and congeners thereof for controlling the growth of unwanted plants

The growth of unwanted plants is controlled by certain cinnoline-4-carboxylic acids and congeners thereof.

Use of 4-(hydroxyiminomethyl)cinnoline and congeners thereof for controlling the growth of unwanted plants

The growth of unwanted plants is controlled by 4-(hydroxyiminomethyl)cinnoline and congeners thereof.