512787-24-5

Basic information

• Product Name: Methanesulfonic acid, trifluoro-, 2-benzoylphenyl ester
• CAS NO: 512787-24-5
• Molecular Formula: C14H9F3O4S
• Molecular Weight: 330.284
• Mol File: 512787-24-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Methanesulfonic acid, trifluoro-, 2-benzoylphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonic acid, trifluoro-, 2-benzoylphenyl ester(512787-24-5)
• EPA Substance Registry System: Methanesulfonic acid, trifluoro-, 2-benzoylphenyl ester(512787-24-5)

Safety Data

• Hazardous Substances Data: 512787-24-5(Hazardous Substances Data)

Upstream product

• 342-62-1 2-benzoylbenzenediazonium tetrafluoroborate 
• 174899-66-2 1-(n-butyl)-3-methylimidazolium triflate 
• 108-95-2 phenol 
• 3117-37-1 3-phenyl-3H-benzofuran-2-one 
• 611-71-2 MANDELIC ACID 
• 117-99-7 2-Hydroxybenzophenone 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 1309688-92-3 C₂₀H₂₁N 
• 1309688-76-3 C₂₈H₁₄F₅NO₂ 
• 1309688-94-5 C₁₈H₁₉NSi 
• 1309688-95-6 C₂₇H₁₉N 
• 1309688-96-7 C₂₈H₂₁N 
• 1309688-98-9 C₂₈H₁₈F₃N 
• 1309689-02-8 C₂₁H₁₅NO 
• 1309688-84-3 C₂₆H₁₈F₅NO₂ 
• 1309688-83-2 C₂₇H₂₀F₅NO₂ 
• 78602-40-1 1-benzylidene-3-phenyl-1H-isoindole 
• 221458-86-2 (phenyl)[2-(2-phenylethynyl)phenyl]methanone 
• 308378-45-2 (2-ethynylphenyl)(phenyl)methanone 
• 172607-53-3 phenyl 2-(trimethylsilylethynyl)phenyl ketone 

Relevant articles and documents

Nickel-Catalyzed Decarbonyloxidation of 3-Aryl Benzofuran-2(3H)-ones to 2-Hydroxybenzophenones

We have developed a protocol to facilitate the nickel-catalyzed decarbonyloxidation of 3-aryl benzofuran-2(3H)-ones to 2-hydroxybenzophenones under mild conditions, which is an efficient approach for the decarbonyloxidation of lactones in organic synthesis. A diverse range of substrates can undergo C(O)-O/C(O)-C bond cleavage to generate the target products in good yields. These 2-hydroxybenzophenones can be converted into a variety of compounds via reactions such as esterification, cyclization, and reduction.

Synthesis of isoindole derivatives by palladium-catalyzed domino reaction of (2-alkynyl)phenylketone o-pentafluorobenzoyloximes

Isoindole derivatives were synthesized by the palladium-catalyzed cyclization of (2-alkynyl)phenylketone O-pentafluoro-benzoyloximes in the presence of organometallic compounds such as sodium formate and aryl boronic acid. Georg Thieme Verlag Stuttgart - New York.

Iron-catalyzed aryl-aryl cross-couplings with magnesium-derived copper reagents

(Chemical Equation Presented) Well-matched couples: Functionalized aryl and heteroaryl copper species obtained from the corresponding magnesium derivatives undergo Fe-catalyzed cross-coupling reactions with aryl iodides that bear keto, ester, triflate, or nitrile groups (see scheme).