15821-13-3

Basic information

• Product Name: 2-methylquinoline-4-carboxamide
• Synonyms: 2-methylquinoline-4-carboxamide;2-Methyl-4-quinolinecarboxamide;Einecs 239-917-8;2-METHYLCINCHONINAMIDE;4-Quinolinecarboxamide, 2-methyl-;Cinchoninamide, 2-methyl-
• CAS NO: 15821-13-3
• Molecular Formula: C₁₁H₁₀N₂O
• Molecular Weight: 186.2099
• EINECS: 239-917-8
• Mol File: 15821-13-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 366.5°C at 760 mmHg
• Flash Point: 175.4°C
• Appearance: /
• Density: 1.227g/cm³
• Vapor Pressure: 1.46E-05mmHg at 25°C
• Refractive Index: 1.658
• CAS DataBase Reference: 2-methylquinoline-4-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylquinoline-4-carboxamide(15821-13-3)
• EPA Substance Registry System: 2-methylquinoline-4-carboxamide(15821-13-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 15821-13-3(Hazardous Substances Data)

Usage

General Description

2-methylquinoline-4-carboxamide is a chemical compound with the molecular formula C11H10N2O. It belongs to the class of organic compounds known as quinoline carboxamides. The compound is a derivative of quinoline, which is a heterocyclic aromatic compound. 2-methylquinoline-4-carboxamide is used in various applications, including as a building block in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, such as its antioxidant and anticancer properties. Additionally, the compound has been investigated for its potential use in organic light-emitting diodes (OLEDs) and organic solar cells.

InChI:InChI=1/C11H10N2O/c1-7-6-9(11(12)14)8-4-2-3-5-10(8)13-7/h2-6H,1H3,(H2,12,14)

Upstream product

• 91-63-4 2-methylquinoline 
• 471-47-6 oxamic acid 
• 77287-34-4 formamide 
• 91-56-5 indole-2,3-dione 
• 67-64-1 acetone 
• 7120-26-5 ethyl 2-methylquinoline-4-carboxylate 
• 55625-40-6 methyl 2-methylquinoline-4-carboxylate 
• 634-38-8 2-methylquinoline-4-carboxylic acid 
• 1076-28-4 2-methylquinoline N-oxide 

Downstream Products

• 29196-15-4 2-methylquinoline-4-carbonitrile 
• 634-38-8 2-methylquinoline-4-carboxylic acid 
• 107518-54-7 2-methyl-quinoline-4-carbonimidic acid anilide 
• 107772-65-6 2-methyl-quinoline-4-carbonimidic acid-(N-methyl-anilide) 
• 107772-66-7 2-methyl-quinoline-4-carbonimidic acid p-toluidide 
• 115400-59-4 (2-methylquinolin-4-yl)(phenyl)methanone 
• 860229-40-9 (2-methyl-1,2,3,4-tetrahydro-[4]quinolyl)-phenyl-methanol 

Relevant articles and documents

Sunlight induced functionalisation of some heterocyclic bases in the presence of polycrystalline TiO2

The functionalisation of various heterocyclic bases induced by sunlight is reported. The photoreaction occurred with higher yield in a liquid-solid heterogeneous system in the presence of polycrystalline TiO2 (anatase) than in a homogeneous system under the same experimental conditions.

NEW SOMATOSTATIN RECEPTOR SUBTYPE 4 (SSTR4) AGONISTS

The invention relates to 3-aza-bicyclo[3.1.0]hexane-6-carboxylic acid amide derivatives of general formula (I), which are agonists of somatostatin receptor subtype 4 (SSTR4), useful for preventing or treating medical disorders related to SSTR4. In addition, the invention relates to processes for preparing pharmaceutical compositions as well as processes for manufacture of the compounds according to the invention.

A novel, selective free-radical carbamoylation of heteroaromatic bases by Ce(IV) oxidation of formamide, catalysed by N-hydroxyphthalimide

The Ce(IV)-NHPI system was used to generate a carbamoyl radical by oxidation of formamide; this nucleophilic radical has been successfully used in the carbamoylation of heteroaromatic bases.