27693-37-4

Usage

Yellow crystalline solid

This describes the physical appearance of the compound, which is a yellow solid with a crystalline structure.

Molecular weight

220.2 g/mol This is the mass of one mole of the compound, which is a measure of its size and stability.

Versatile reactivity

This refers to the compound's ability to undergo chemical reactions with a variety of other compounds, making it useful in the synthesis of pharmaceuticals and organic compounds.

Application in the production of dyes, pigments, and other organic materials

This indicates that the compound is used in the production of various materials, including dyes and pigments, due to its chemical properties.

Potential medicinal properties

This suggests that the compound has been studied for its potential therapeutic uses, including as an anti-inflammatory and antiviral agent.

Practical applications in the fields of chemistry, pharmaceuticals, and materials science

This highlights the compound's relevance and use in various scientific fields, making it an important chemical compound.

InChI:InChI=1/C12H8N2O3/c15-12(10-6-3-4-8-13-10)9-5-1-2-7-11(9)14(16)17/h1-8H

Upstream product

• 98-98-6 2-Picolinic acid 
• 99-61-6 3-nitro-benzaldehyde 
• 91-02-1 phenyl(pyridin-2-yl)methanone 
• 104621-62-7 2‐(3‐nitrobenzyl)pyridine 
• 941279-81-8 2,4-dimethyl-3-(pyridin-2-ylmethyl)pentan-3-ol 
• 109-06-8 α-picoline 

Downstream Products

• 121-92-6 3-nitrobenzoic acid 
• 23724-01-8 trans-RhCl₂(OH)(m-O₂NC₆H₄COpy)2 
• 23361-01-5 trans-{RhCl₂(m-O₂NC₆H₄COpy)2}(ClO₄) 
• 73742-08-2 2-(3-aminobenzoyl)pyridine 

Relevant academic research and scientific papers

Synthesis of aryl(di)azinyl ketones through copper- and iron-catalyzed oxidation of the methylene group of aryl(di)azinylmethanes

Sustainable Oxidations: An oxidation method to transform aryl(di)azinylmethanes into aryl(di)azinyl ketones is described. Base metals (copper and iron) as catalysts in combination with O2 as the oxidant are used, which makes this method sustainable. The utility of this method is illustrated by the synthesis of 6-(4-methylbenzoyl)pyridine-2-carbaldehyde, which is an intermediate in the preparation of the drug Acrivastine. Copyright

1H,3H-PYRROL[1,2-c]THIAZOLE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

A compound of the general formula I; STR1 in which R is hydrogen or a halogen or an alkyl, alkyloxy, alkylthio, trifluoromethyl, amino, alkylamino, dialkylamino, hydroxy, cyano, carboxy, alkylsulphinyl, alkylsulphonyl, sulphamido, alkylsulphamido, dialkylsulphamido, carbamoyl, alkylcarbamoyl, dialkylcarbamoyl, phenylcarbamoyl, diphenylcarbamoyl, pyridylcarbamoyl, dipyridylcarbamoyl, benzyl, alkylcarbonyl, benzoyl, alkyloxycarbonyl, phenoxycarbonyl, alkylcarbonyloxy, benzoyloxy, alkylcarbonylamino, benzamido, phenyl, phenoxy or phenylthio group, X is oxygen or sulphur or an imino, alkylimino, phenylimino, benzylimino, sulphinyl, sulphonyl, carbonyl, carbonylmethylene, methylenecarbonyl, carbonylvinylene or vinylenecarbonyl group, or X represents a valency bond or a straight-chain alkylene group containing 1 to 4 carbon atoms and Ar is a phenyl, naphthyl, pyridyl, quinolinyl, isoquinolinyl, thienyl, benzothienyl, thieno 3,2-b!thien-2-yl or thieno 2,3-b!thien-2-yl group, it being possible for the group Ar to be unsubstituted or substituted with one or more halogen or alkyl, alkyloxy, alkylthio, trifluoromethyl, amino, alkylamino, dialkylamino, hydroxy, cyano, carboxy, alkylsulphinyl, alkylsulphonyl, sulphamido, alkylsulphamido, dialkylsulphamido, carbamoyl, alkylcarbamoyl, dialkylcarbamoyl, phenylcarbamoyl, diphenylcarbamoyl, pyridylcarbamoyl, dipyridylcarbamoyl, benzyl, alkylcarbonyl, benzoyl, alkyloxycarbonyl, phenoxycarbonyl, alkylcarbonyloxy, benzoyloxy, alkylcarbonylamino or benzamido group;each alkyl moiety containing 1 to 4 straight-or branched-chain carbon atoms; the compound being in separate enantiomeric form or mixtures thereof or a pharmaceutically acceptable salt thereof is useful in the treatment of all the pathological conditions in which PAF-acether may be directly or indirectly implicated.