1417782-28-5

Basic information

• Product Name: 1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one
• Synonyms: 1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one
• CAS NO: 1417782-28-5
• Molecular Weight: 314.691
• Mol File: 1417782-28-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 372.5±42.0 °C(Predicted)
• Density: 1.327±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one(1417782-28-5)
• EPA Substance Registry System: 1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one(1417782-28-5)

Safety Data

• Hazardous Substances Data: 1417782-28-5(Hazardous Substances Data)

Usage

General Description

1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one is a chemical compound with a structure consisting of a phenyl ring attached to an ethanone group, with a trifluoromethyl group and a 4-chlorophenoxy group. It is a ketone compound that may be used in various chemical and pharmaceutical applications. The presence of the chlorophenoxy and trifluoromethyl groups could impart specific properties to the compound, making it useful in certain chemical reactions or as a building block for synthesizing other compounds. The distinct structural features of this chemical can also make it an interesting target for further research and exploration in the field of organic chemistry.

Upstream product

• 106-46-7 para-dichlorobenzene 
• 1096960-88-1 C₁₄H₇ClF₃NO 
• 108-59-8 malonic acid dimethyl ester 
• 320-42-3 4-hydroxy-2-(trifluoromethyl)benzonitrile 
• 320-47-8 4-nitro-2-trifluoromethylbenzonitrile 
• 79756-81-3 (+/-)-α-(o-(trifluoromethyl)phenyl)ethyl alcohol 
• 106-48-9 4-chloro-phenol 
• 208173-21-1 1-(4-fluoro-2-(trifluoromethyl)phenyl)ethan-1-one 
• 1417782-30-9 1-bromo-4-(4-chlorophenoxy)-2-(trifluoromethyl)benzene 
• 75-36-5 acetyl chloride 
• 40161-55-5 1-bromo-4-fluoro-2-(trifluoromethyl)benzene 

Downstream Products

• 1417782-29-6 2-[4-(4-chloro-phenoxy)-2-trifluoromethyl-phenyl]-2-methyl-oxirane 
• 1417782-03-6 (2RS)-2-[4-(4-chlorophenoxy)-α,α,α-trifluoro-o-tolyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol 
• 1417782-22-9 2-bromo-1-[4-(4-chloro-phenoxy)-2-trifluoromethyl-phenyl]-ethanone 
• 1417782-23-0 1-[4-(4-chloro-phenoxy)-2-trifluoromethyl-phenyl]-2-[1,2,4]triazol-1-yl-ethanone 
• 1417782-04-7 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol 
• 1417782-11-6 1-[2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-2-methoxy-propyl]-1,2,4-triazole 
• 1417782-19-4 1-[2-allyloxy-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)-phenyl]propyl]-1,2,4-triazole 
• 1417782-07-0 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)pent-3-yn-2-ol 
• 1417782-10-5 1-[2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-2-methoxy-butyl]-1,2,4-triazole 

Relevant articles and documents

Method for preparing meconazole intermediate

The invention relates to a preparation technology of a bactericide, namely, meconazole, and discloses a method for preparing a compound shown as a formula (I), which comprises the following steps: (1) in the presence of organic alkali, contacting a compound shown as a formula (II) with a compound shown as a formula (III) for a condensation reaction; and (2) sequentially carrying out hydrolysis reaction I and decarboxylation reaction on a product obtained after the condensation reaction to obtain the compound shown in the formula (I). In the process for preparing the compound as shown in the formula (I), a Grignard reagent is not used, the cost of raw materials is effectively reduced, three wastes generated in the process are reduced, meanwhile, the total yield of the reaction is high, and the method is suitable for industrial mass production. .

AGENT FOR AGRICULTURAL AND HORTICULTURAL USE, PLANT DISEASE CONTROL METHOD, AND PLANT DISEASE CONTROL PRODUCT

PROBLEM TO BE SOLVED: To provide an agent for agricultural and horticultural use in which the content of active ingredients can be reduced. SOLUTION: An agent for agricultural and horticultural use contains an active ingredient and an adjuvant, the active ingredient being a compound represented by formula (Ia), or an N-oxide thereof or an agro-pharmaceutically acceptable salt thereof, the adjuvant being alkyl glycoside (R7 is a C1-C6-alkyl group; R3 is a halogen group, a C1-C4-alkyl group, a C1-C4-haloalkyl group or a C1-C4-alkoxy group; R4 is H, a halogen group, a phenyl group, a phenyl-oxy group, a C1-C4-haloalkyl group or a C1-C4-haloalkoxy group). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPO&INPIT

PROCESS FOR THE PREPARATION OF SUBSTITUTED ARYL KETONES

The present invention relates to a process for providing substituted aryl ketones.Furthermore, the invention relates to intermediates of said process and the use of substituted aryl ketones obtained by the inventive process for the preparation of triazole