1036762-58-9

Basic information

• Product Name: P-Trifluoromethyl phenyl acetonite
• Synonyms: P-Trifluoromethyl phenyl acetonite
• CAS NO: 1036762-58-9
• Molecular Formula: C₁₀H₉F₃O₂
• Molecular Weight: 218.17
• Mol File: 1036762-58-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: P-Trifluoromethyl phenyl acetonite(CAS DataBase Reference)
• NIST Chemistry Reference: P-Trifluoromethyl phenyl acetonite(1036762-58-9)
• EPA Substance Registry System: P-Trifluoromethyl phenyl acetonite(1036762-58-9)

Safety Data

• Hazardous Substances Data: 1036762-58-9(Hazardous Substances Data)

Upstream product

• 402-45-9 4-hydroxybenzotrifluoride 
• 78-95-5 chloroacetone 

Downstream Products

• 247200-01-7 C₁₁H₁₁F₃N₂O 
• 89763-86-0 1-methyl-2-(p-(trifluoromethyl)phenoxy)ethylamine 

Relevant articles and documents

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

Design, synthesis and effect of the introduction of a propargyloxy group on the fungicidal activities of 1-substituted phenoxypropan-2-amino valinamide carbamate derivatives

The cell walls of oomycetes are composed of cellulose, making cellulose synthase enzymes good targets for carboxylic acid amide fungicides. Valinamide carbamates are amino acid fungicides that represent excellent alternatives to conventional synthetic pesticides in terms of their ability to reduce the negative impacts of these compounds on human health and the environment. In a continuation of our research towards the development of new cellulose synthase inhibitors, we have developed a series of "stretched" analogues of iprovalicarb by the introduction of an additional OCH2 linker. The bioassay results indicated that compounds containing a small group at the para-position of phenyl gave excellent fungicidal activities with EC50 values ranging from 0.59 to 2.06 μmol L-1. Most notably, the introduction of a propargyloxy group led to a pronounced increase in the fungicidal activity. Furthermore, compound 7o bearing a propargyloxy group was identified as the most promising candidate because of its excellent fungicidal potency against oomycete diseases and good fungicidal activity against non-oomycete diseases.