131088-90-9

Basic information

• Product Name: α-[2H1]p-fluorotoluene
• Synonyms: α-[2H1]p-fluorotoluene
• CAS NO: 131088-90-9
• Molecular Weight: 111.123
• Mol File: 131088-90-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: α-[2H1]p-fluorotoluene(CAS DataBase Reference)
• NIST Chemistry Reference: α-[2H1]p-fluorotoluene(131088-90-9)
• EPA Substance Registry System: α-[2H1]p-fluorotoluene(131088-90-9)

Safety Data

• Hazardous Substances Data: 131088-90-9(Hazardous Substances Data)

Upstream product

• 7116-50-9 1-fluoro-4-methoxymethyl-benzene 
• 405-50-5 p-Fluorophenylacetic acid 
• 131089-00-4 4‐fluorophenyl‐[²H]‐methanol 
• 459-57-4 4-fluorobenzaldehyde 
• 131089-01-5 α-<2H1>p-fluorobenzyl chloride 

Relevant articles and documents

Method for preparing deuterated compound through decarboxylation and deuteration of carboxylic acid

The invention relates to a method for preparing a deuterated compound through decarboxylation and deuteration of carboxylic acid. According to the method, a carboxylic acid compound is used as a raw material, hydrogen atoms of carboxylate radicals are exc

Side Chain Hydroxylation of Aromatic Compounds by Fungi. Part 4. Influence of the para Substituent on Kinetic Isotope Effects During Benzylic Hydroxylation by Mortierella isabellina

The benzylic hydroxylation of a series of para-substituted toluenes by the fungus Mortierella isabellina has been studied by using CD3, CHD2, and CH2D methyl labelled substrates.Inter- and intramolecular primary and secondary deuterium kinetic isotope effect ratios have been determined: the intermolecular primary effects are maximal with strongly electron-withdrawing para substituents (R = CN and CF3), while the intramolecular primary effects are minimal for R = H but increase in instances where R is electron donating or withdrawing.These results are interpreted in terms of a dependence of the hydroxylation mechanism on the nature of the para substituent.