68359-53-5

Usage

Uses

Used in Pharmaceutical Industry:
M-Phenoxy-P-Fluorobenzyl Alcohol is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical properties, including the presence of the fluoro group, make it a valuable component in the development of new drugs.
Used in Agrochemical Production:
M-Phenoxy-P-Fluorobenzyl Alcohol is used as a key ingredient in the formulation of agrochemical products. Its reactivity and solubility properties contribute to the effectiveness of these products in agricultural applications.
Used in Organic Chemistry Research:
M-Phenoxy-P-Fluorobenzyl Alcohol is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studies on chemical reactions and synthesis.
Used in Medicinal Chemistry:
M-Phenoxy-P-Fluorobenzyl Alcohol is used as a building block in the design and synthesis of new medicinal compounds. Its presence in the molecular structure can influence the pharmacological properties of the resulting drug candidates.
Used in Material Science:
M-Phenoxy-P-Fluorobenzyl Alcohol is used in the development of new materials with specific properties. Its chemical characteristics can contribute to the creation of materials with improved performance in various applications.

InChI:InChI=1/C13H11FO2/c14-12-7-6-10(9-15)8-13(12)16-11-4-2-1-3-5-11/h1-8,15H,9H2

Upstream product

• 68359-57-9 4-fluoro-3-phenoxybenzaldehyde 

Downstream Products

• 75210-42-3 (4-fluoro-3-phenoxyphenyl)methyl chloride 
• 83492-87-9 3-Phenoxy-4-fluorobenzyl 2-(3-methylphenyl)-2-methylpropyl ether 
• 76725-69-4 2,2-dimethyl-3-(2-chloro-2-(4-methoxyphenyl)-vinyl)-cyclopropanecarboxylic acid (4-fluoro-3-phenoxy-benzyl)-ester 
• 84385-70-6 4-fluoro-3-phenoxybenzyl 2-(1-hepten-1-yl)-3-3-dimethylcyclopropanecarboxylate 
• 83492-86-8 3-phenoxy-4-fluorobenzyl 2-(4-chlorophenyl)-2-methylpropyl ether 

Relevant academic research and scientific papers

IRIDIUM-BASED CATALYSTS FOR HIGHLY EFFICIENT DEHYDROGENATION AND HYDROGENATION REACTIONS IN AQUEOUS SOLUTION AND APPLICATIONS THEREOF

A series of iridium-based catalysts for dehydrogenation of formic acid, and hydrogenation using formic acid as the hydrogen source, and the process using the catalyst(s) to produce hydrogen gas from formic acid solution, or to reduce aldehydes using formic acid, are disclosed and claimed. More specifically, the present invention relates to a group of pentamethylcyclopentadienyl (Cp*) iridium complexes with different Ν,Ν-bidentate ligands that catalyze dehydrogenation from formic acid, and chemo-selective hydrogenation of aldehydes, in the aqueous solution system in a highly efficient, and long life-time manner.

Iridium-catalyzed highly efficient chemoselective reduction of aldehydes in water using formic acid as the hydrogen source

A water-soluble highly efficient iridium catalyst is developed for the chemoselective reduction of aldehydes to alcohols in water. The reduction uses formic acid as the traceless reducing agent and water as a solvent. It can be carried out in air without the need for inert atmosphere protection. The products can be purified by simple extraction without any column chromatography. The catalyst loading can be as low as 0.005 mol% and the turn-over frequency (TOF) is as high as 73 800 mol mol-1 h-1. A wide variety of functional groups, such as electron-rich or deficient (hetero)arenes and alkenes, alkyloxy groups, halogens, phenols, ketones, esters, carboxylic acids, cyano, and nitro groups, are all well tolerated, indicating excellent chemoselectivity.

1,4-diaryl-1-cyclopropyl-4-substituted butanes as insecticides and acaricides

The 1,4-diaryl-1-cyclopropyl-4-substituted butane pesticides of the following formula are effective as insecticides and acaricides: STR1 in which X and Y are independently hydrogen, halogen, alkyl, alkoxy, cycloalkylalkoxy, alkylcarbonyl, alkoxycarbonyl,

Insecticidal cyclopropyl di(aryl) 2-butenes

Compounds of the formula STR1 in which Ar is substituted or unsubstituted phenyl, naphthyl, or thienyl; and Ar1 is 3-phenoxyphenyl, 4-fluoro-3-phenoxyphenyl, 2-methyl[1-1'-biphenyl]-3-yl, or 6-phenoxy-2-pyridyl, exhibit pyrethroid-like insectic

Insecticidal cyclopropyl-substituted di(aryl) compounds

Compounds of the formula STR1 in which Ar is substituted or unsubstituted phenyl, naphthyl, or thienyl; Z is oxygen, sulfur, or methylene; and Ar' is 2-methyl[1,1'-biphenyl]-3-yl, 3-phenoxyphenyl, 4-fluoro-3-phenoxyphenyl, or 6-phenoxy-2-pyridyl exhibit pyrethroid-like insecticidal and acaricidal activity and are relatively harmless to aquatic fauna.

Substituted phenyltrialkylsilane insecticides

Compounds of the formula STR1 in which Ar is substituted or unsubstituted phenyl, pyridinyl, furanyl, naphthyl, thienyl, or thiazolyl; R is a (C1-4) alkyl; W is oxygen or methylene; and Ph is substituted or unsubstituted phenoxyphenyl, benzylph

Pyrimidine substituted-2,2-dimethylcyclopropane carboxylates useful for combating insect and acarine pests at a locus

A compound of formula: STR1 wherein R2 represents an α-branched alkyl group containing from 3 to 6 carbon atoms, and R represents either (a) hydroxy, halo or alkoxy of up to six carbon atoms, or (b) the group --OR1 where R1 is the residue of an alcohol of formula R1 OH which forms an insecticidal ester with chrysanthemic acid, permethrin acid or cyhalothrin acid. The compounds have insecticidal and acaricidal properties.

Substituted phenyltrialkylsilane insecticides

Compounds containing a dimethylsilane core and a phenoxybenzyl substituent are found to exhibit pyrethroid-like activity toward insects with low toxicity to fish.