4958-56-9

Usage

Uses

Used in Ink Production:
2-METHYLAMINO-5-NITROBENZOPHENONE is used as a photoinitiator for the production of inks, enabling the curing process through the absorption of ultraviolet light and initiation of polymerization reactions.
Used in Adhesive Manufacturing:
In the adhesive industry, 2-METHYLAMINO-5-NITROBENZOPHENONE serves as a photoinitiator, facilitating the curing of adhesives by initiating polymerization upon exposure to ultraviolet light.
Used in Coating Production:
2-METHYLAMINO-5-NITROBENZOPHENONE is utilized as a photoinitiator in the manufacturing of coatings, promoting the curing process through the absorption of ultraviolet light and the initiation of polymerization reactions.
It is crucial to handle and store 2-METHYLAMINO-5-NITROBENZOPHENONE with care, as it is classified as a hazardous chemical. Proper management is necessary to prevent skin and eye irritation or other potential adverse health effects.

InChI:InChI=1/C14H12N2O3/c1-15-13-8-7-11(16(18)19)9-12(13)14(17)10-5-3-2-4-6-10/h2-9,15H,1H3

Upstream product

• 2011-67-8 nimetazepam 
• 1217315-74-6 3-benzoyl-2-methyl-5-nitropyridine 
• 1335201-81-4 C₁₄H₁₃N₂O₃⁽¹⁺⁾*ClO₄^(1-) 
• 74-89-5 methylamine 
• 1335201-71-2 1-methyl-5-nitro-2-(2-oxo-2-phenylethyl)pyridinium perchlorate 
• 1335201-72-3 [2-methyl-5-nitropyrid-2(1H)-ylidene]acetophenone 
• 69639-75-4 Dimethylammonium sulphite 
• 93-89-0 benzoic acid ethyl ester 
• 1279130-86-7 2-(5-nitropyridin-2-yl)-1-phenylethanone 
• 102725-60-0 {[1-(2-Methylamino-5-nitro-phenyl)-1-phenyl-meth-(Z)-ylidene]-amino}-acetic acid 

Downstream Products

• 2011-67-8 nimetazepam 

Relevant academic research and scientific papers

A new synthetic route to benzophenone derivatives

The rearrangement reaction of 1-alkyl-2-(benzoylmethyl)pyridinium iodides 3a-d, 6 in the presence of various nucleophiles leads to 2-alkylaminobenzophenone derivatives 4a-c. Best results were achieved with alkylammonium sulfites as recyclization reagents.

Nitropyridines 11.* recyclization of quaternary nitropyridinium salts into substituted nitroanilines

Substituted nitroanilines have been obtained by the recyclization of nitropyridinium quaternary salts under the action of bases.

Micellar Catalysis of Organic Reactions. 18. Basic Hydrolysis of Diazepam and Some N-Alkyl Derivatives of Nitrazepam

Kinetic and mechanistic studies of the basic hydrolysis of several benzodiazepinone drugs have been carried out in the presence of micelles of cetyltrimethylammonium bromide (CTAB) and in aqueous solution.For diazepam, a change of mechanism from initial azomethine hydrolysis in water to initial amide hydrolysis in the presence of micelles of CTAB is indicated.For nimetazepam and N-benzylnitrazepam, initial amide hydrolysis was observed both in the presence of CTAB and in water.For the latter compounds, strong catalysis (50-100) of amide hydrolysis (phase 1) by micelles of CTAB was observed, while azomethine hydrolysis (phase 2) was only very weakly catalyzed (3-4-fold).For diazepam, the catalysis was smaller (9-18-fold), but this was accompanied by a mechanistic change so that here the actual catalysis of amide hydrolysis is masked.