57872-48-7

Basic information

• Product Name: ketoprofen methyl ester
• CAS NO: 57872-48-7
• Molecular Weight: 268.312
• Mol File: 57872-48-7.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: ketoprofen methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ketoprofen methyl ester(57872-48-7)
• EPA Substance Registry System: ketoprofen methyl ester(57872-48-7)

Safety Data

• Hazardous Substances Data: 57872-48-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 22071-15-4 ketoprofen 
• 201230-82-2 carbon monoxide 
• 80622-53-3 methyl 2-(3-bromophenyl)propanoate 
• 98-80-6 phenylboronic acid 
• 1218999-64-4 methyl 2-(3-iodophenyl)propanoate 
• 71-43-2 benzene 
• 1016-77-9 3-bromobenzophenone 
• 119-61-9 benzophenone 
• 5445-17-0 Methyl 2-bromopropionate 
• 118633-39-9 Benzoesaeure--anhydrid 
• 142569-76-4 methyl 2-(2-iodophenyl)propionate 
• 22161-81-5 S-ketoprofen 
• 108-86-1 bromobenzene 

Downstream Products

• 22161-81-5 S-ketoprofen 
• 56105-81-8 R-ketoprofen 
• 856893-03-3 2-(3-benzoylphenyl)-3-methoxy-2-methylpropionic acid methyl ester 
• 321879-84-9 methyl 2-[3-(2-phenyl-1,3-dioxolan-2-yl)phenyl]propionate 
• 461382-61-6 2,2'-(3-benzoyl-phenyl)-methylhexanoic acid 
• 1073126-84-7 2-(3-benzoylphenyl)propanehydrazide 
• 22071-15-4 ketoprofen 
• 1260498-36-9 methyl 2-(3-benzoylphenyl)-2-methylpentanoate 
• 24021-59-8 methyl -2--(3--benzoylphenyl)--2--methylpropanoate 
• 1262801-26-2 3-[2-{5-(1-(3-benzoylphenyl)ethyl)-1,3,4-oxadiazol-2-ylthio}acetyl]-2H-chromen-2-one 
• 1262801-32-0 C₁₇H₁₄N₂O₂S 

Relevant articles and documents

Green Esterification of Carboxylic Acids Promoted by tert-Butyl Nitrite

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CHEMOSELECTIVE METHYLENE HYDROXYLATION IN AROMATIC MOLECULES

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Ni-Catalyzed Reductive C-O Bond Arylation of Oxalates Derived from α-Hydroxy Esters with Aryl Halides

A Ni-catalyzed reductive cross-coupling of α-hydroxycarbonyl compounds modified with oxalyl groups and aryl halides has been developed that furnishes α-aryl esters under mild conditions and tolerates a variety of functionalized aryl halides bearing electron-withdrawing and -donating groups. This work highlights C-O bond fragmentation on secondary alkyl carbon centers that generates α-carbonyl radicals.