62451-84-7

Basic information

• Product Name: METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE
• Synonyms: (3-TRIFLUOROMETHYLPHENYL) ACETIC ACID METHYL ESTER;METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE;AURORA KA-6005;Methyl 3-(trifluoromethyl)phenylacetate 97%;Methyl 3-(trifluoromethyl)phenylacetate,97%;Methyl 2-[3-(trifluoromethyl)phenyl]acetate;3-(Trifluoromethyl)phenylacetic acid methyl ester, 3-(2-Methoxy-2-oxoethyl)benzotrifluoride;Methyl 2-(3-(trifluoromethyl)
• CAS NO: 62451-84-7
• Molecular Formula: C₁₀H₉F₃O₂
• Molecular Weight: 218.17
• Mol File: 62451-84-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 211℃
• Flash Point: 60.8 °C
• Appearance: Clear colorless/Liquid
• Density: 1.24
• Vapor Pressure: 0.187mmHg at 25°C
• Refractive Index: 1.45-1.452
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE(62451-84-7)
• EPA Substance Registry System: METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE(62451-84-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26
• HazardClass: IRRITANT
• Hazardous Substances Data: 62451-84-7(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless liquid

InChI:InChI=1/C10H9F3O2/c1-15-9(14)6-7-3-2-4-8(5-7)10(11,12)13/h2-5H,6H2,1H3

Upstream product

• 186581-53-3 diazomethane 
• 351-35-9 3-(trifluoromethyl)phenylacetic acid 
• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 96-34-4 methyl chloroacetate 
• 349-75-7 3-(trifluoromethyl)benzyl alcohol 
• 67-56-1 methanol 
• 1360789-05-4 1-(2,2,6,6-tetramethylpiperidin-1-yl)-2-(3-(trifluoromethyl)phenyl)ethanone 
• 454-92-2 3-(trifluoromethyl)benzoic acid 
• 30359-53-6 3-trifluoromethyl-β,β,β-trichloro-ethylbenzene 
• 2338-76-3 3-trifluoromethylphenylacetonitrile 
• 705-29-3 3-Trifluoromethylbenzyl chloride 

Downstream Products

• 138485-29-7 2-[3-(trifluoromethyl)phenyl]malonic acid-1,3-dimethyl ester 
• 619323-19-2 2-(3-trifluoromethyl-phenyl)-pent-4-enoic acid methyl ester 
• 89768-05-8 1-Cyano-1-phenyl-3-(3-trifluoromethylphenyl)-2-propanone 
• 71792-93-3 1,3-bis(3-(trifluoromethyl)phenyl)propan-2-one 
• 1383916-52-6 bis(2,4,6‐trichlorophenyl)-2‐(3‐(trifluoromethyl)phenyl)malonate 
• 89744-95-6 methyl 2-(3-(trifluoromethyl)phenyl)acrylate 
• 1361319-26-7 methyl 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-2-[3-(trifluoromethyl)phenyl]propanoate 
• 1280732-89-9 2-(3-trifluoromethyl-benzyl)-[1,3,4]oxadiazole 
• 1123196-19-9 1-amino-3-(3-trifluoromethylphenyl)piperidin-2-one 

Relevant articles and documents

Discovery of Novel Benzo[4,5]thiazolo(oxazolo)[3,2-a]pyrimidinone Mesoionic Derivatives as Potential Antibacterial Agents and Mechanism Research

A series of benzo[4,5]thiazole(oxazole)[3,2-a]pyrimidine mesoionic compounds were designed and synthesized. Antibacterial activity tests revealed that compound A23 showed good in vitro activities against Xanthomonas oryzae pv. Oryzicola (Xoc) and Xanthomo

Novel mesoionic compound and synthesis and application thereof

The invention discloses a novel mesoionic compound and synthesis and application thereof, and particularly discloses a novel mesoionic compound as shown in a formula (I), wherein X is CH or N. A Is phenyl. Naphthyl, 1,3 -benzodiazole -5 - base and C1

Efficient Synthesis of Spirooxindole Pyrrolones by a Rhodium(III)-Catalyzed C?H Activation/Carbene Insertion/Lossen Rearrangement Sequence

A rhodium(III)-catalyzed domino annulation of simple olefins with diazo oxindoles to give spirooxindole pyrrolone products is described. This reaction can be formally viewed as the result of an anomalous tandem C?H activation, carbene insertion, Lossen rearrangement, and a nucleophilic addition process. The potential utility of this reaction was further demonstrated by the late-stage diversification of drug molecules.