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

Description

1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one is a complex organic ketone compound characterized by a phenyl ring with a trifluoromethyl group and a 4-chlorophenoxy group attached to it. This unique molecular structure endows the compound with specific properties that make it a versatile building block in chemical and pharmaceutical applications.

Uses

Used in Chemical Synthesis:
1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one is used as a key intermediate in the synthesis of various organic compounds. Its distinct structural features, including the trifluoromethyl and 4-chlorophenoxy groups, make it a valuable precursor for the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one is used as a building block for the development of pharmaceutical compounds. The presence of the chlorophenoxy and trifluoromethyl groups can impart specific biological activities to the synthesized compounds, making them potential candidates for drug discovery and development.
Used in Research and Development:
1-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)ethan-1-one is used as a research target in the field of organic chemistry. Its unique molecular structure and potential reactivity make it an interesting subject for further exploration and investigation, leading to the discovery of new chemical reactions and applications.

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