265299-13-6

Basic information

• Product Name: methyl 2-(acetoxy(4-fluorophenyl)methyl)acrylate
• Synonyms: methyl 2-(acetoxy(4-fluorophenyl)methyl)acrylate
• CAS NO: 265299-13-6
• Molecular Weight: 252.242
• Mol File: 265299-13-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: methyl 2-(acetoxy(4-fluorophenyl)methyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(acetoxy(4-fluorophenyl)methyl)acrylate(265299-13-6)
• EPA Substance Registry System: methyl 2-(acetoxy(4-fluorophenyl)methyl)acrylate(265299-13-6)

Safety Data

• Hazardous Substances Data: 265299-13-6(Hazardous Substances Data)

Upstream product

• 459-57-4 4-fluorobenzaldehyde 
• 75-36-5 acetyl chloride 
• 353506-65-7 methyl 3-(4-fluorophenyl)-3-hydroxy-2-methylenepropanoate 
• 108-24-7 acetic anhydride 

Downstream Products

• 914979-64-9 3-(4-fluorophenyl)-2-methylene-4-nitro-pentanoic acid methyl ester 
• 914979-59-2 3-(4-fluorophenyl)-2-methylene-4-nitro-pentanedioic acid 5-ethyl ester 1-methyl ester 
• 910641-59-7 2-cyano-3-(4-fluoro-phenyl)-4-methylene-pentanedioic acid 1-ethyl ester 5-methyl ester 
• 1038998-50-3 3-(4-fluorobenzyl)-7,8-dihydro-6H-chromene-2,5-dione 
• 1000697-56-2 3-(4-fluorobenzyl)-7,7-dimethyl-7,8-dihydro-6H-chromene-2,5-dione 
• 1082208-20-5 methyl (E)-2-((1H-1,2,4-triazol-1-yl)methyl)-3-(4-fluorophenyl)acrylate 
• 1082208-21-6 methyl 2-((4-fluorophenyl)(1H-1,2,4-triazol-1-yl)methyl)acrylate 
• 1149760-03-1 (E)-1-tert-butyl 5-methyl 2-(diphenylmethyleneamino)-4-(4-fluorobenzylidene)pentanedioate 
• 1186205-18-4 1-methyl 5-ethyl 2-[(E)-(4-fluorophenyl)methylidene]-4-nitropentanedioate 
• 1189520-17-9 (E)-5-(4-fluorobenzylidene)-2-(3-methoxyphenyl)-5,6-dihydropyrimidin-4(3H)-one 
• 1190585-93-3 methyl 2-((4-fluorophenyl)(phenylamino)methyl)acrylate 
• 1009375-48-7 (E)-methyl 2-(aminomethyl)-3-(4-fluorophenyl)acrylate 

Relevant articles and documents

Novel organophosphorus scaffolds of urease inhibitors obtained by substitution of Morita-Baylis-Hillman adducts with phosphorus nucleophiles

The reactivity of Morita-Baylis-Hillman allyl acetates was employed to introduce phosphorus-containing functionalities to the side chain of the cinnamic acid conjugated system by nucleophilic displacement. The proximity of two acidic groups, the carboxyla

Synthesis, characterization and antimicrobial activity of some new Baylis-Hillman derived benzothiazolo pyrimidinone derivatives

A series of Baylis-Hillman derived 22 new benzothiazolo pyrimidinone derivatives have been synthesized from Baylis-Hillman acetates and 2-amino benzothiazole under neat conditions with high yields. All the newly synthesized compounds have been characteriz

Application of primary allylamines from morita-baylis-hillman adducts: Cyanogen azide mediated synthesis of substituted 5-aminotetrazoles and their attempted transformation into tetrazolo[1,5-a]pyrimidinones

A general protocol for the synthesis of substituted 5-aminotetrazoles by treating cyanogen azide with primary allylamines afforded either by S N2 or SN2′ reactions of Morita- Baylis-Hillman acetates of acrylate has been developed. Th