68359-53-5

Basic information

• Product Name: M-PHENOXY-P-FLUOROBENZYL ALCOHOL
• Synonyms: RARECHEM AL BD 1188;M-PHENOXY-P-FLUOROBENZYL ALCOHOL;(4-FLUORO-3-PHENOXY-PHENYL)-METHANOL;3-(PHENOXY)-4-FLUORO-BENZYL ALCOHOL;M-Phenoxy-P-Fluoro-Benzoic Alcohol;p-Fluoro-m-phenoxybenzyl alcohol;m-Phenoxy -4-fluorobenzyl alcohol
• CAS NO: 68359-53-5
• Molecular Formula: C₁₃H₁₁FO₂
• Molecular Weight: 218.22
• Mol File: 68359-53-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 317.8oC at 760 mmHg
• Flash Point: 149.8oC
• Appearance: /
• Density: 1.225g/cm3
• Vapor Pressure: 0.000158mmHg at 25°C
• Refractive Index: 1.578
• Storage Temp.: 2-8°C
• PKA: 13.94±0.10(Predicted)
• CAS DataBase Reference: M-PHENOXY-P-FLUOROBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: M-PHENOXY-P-FLUOROBENZYL ALCOHOL(68359-53-5)
• EPA Substance Registry System: M-PHENOXY-P-FLUOROBENZYL ALCOHOL(68359-53-5)

Safety Data

• Hazardous Substances Data: 68359-53-5(Hazardous Substances Data)

Usage

General Description

M-Phenoxy-P-Fluorobenzyl Alcohol is a synthetic, organic compound known for its role in the pharmaceutical industry and in the production of agrochemical products. It belongs to a class of compounds called phenoxy alcohols, which are characterized by a phenolic ring and an alcohol functional group. The presence of the fluoro group at the para position enhances its reactivity and improves its solubility. Despite limited direct information regarding this specific chemical, similar compounds show promise in research within several different fields, including organic chemistry, medicinal chemistry and material science due to their unique chemical properties. However, like many chemicals, it should be handled with caution as it may pose health risks upon exposure.

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 
• 83492-86-8 3-phenoxy-4-fluorobenzyl 2-(4-chlorophenyl)-2-methylpropyl ether 
• 84385-70-6 4-fluoro-3-phenoxybenzyl 2-(1-hepten-1-yl)-3-3-dimethylcyclopropanecarboxylate 
• 76725-69-4 2,2-dimethyl-3-(2-chloro-2-(4-methoxyphenyl)-vinyl)-cyclopropanecarboxylic acid (4-fluoro-3-phenoxy-benzyl)-ester 

Relevant articles and documents

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.

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-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.