58908-97-7

Basic information

• Product Name: Phenol, 4-(3-methylphenoxy)-
• Synonyms: 4-m-Tolyloxy-phenol;O-m-Tolyl-hydrochinon;p-(m-tolyloxy)phenol;p-(3-methylphenoxy)-phenol;4-Hydroxy-1-m-tolyloxy-benzol;4-Hydroxyphenyl-8-methylphenylether;(4-Hydroxy-phenyl)-m-tolyl-aether;Phenol,4-(3-methylphenoxy)
• CAS NO: 58908-97-7
• Molecular Formula: C13H12O2
• Molecular Weight: 200.23300
• Mol File: 58908-97-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 4-(3-methylphenoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-(3-methylphenoxy)-(58908-97-7)
• EPA Substance Registry System: Phenol, 4-(3-methylphenoxy)-(58908-97-7)

Safety Data

• Hazardous Substances Data: 58908-97-7(Hazardous Substances Data)

Upstream product

• 82721-04-8 1-(4-methoxyphenoxy)-3-methylbenzene 
• 67073-91-0 2,4,6-Tri-tert-butyl-4-m-tolyloxy-cyclohexa-2,5-dienone 

Downstream Products

• 85983-22-8 2-[p-(m-tolyloxy)phenoxy]-ethanol 
• 119551-63-2 1-{[p-(3-methyl)-phenoxyphenoxy]-methyl}-1,2,4-triazole 
• 40843-29-6 2-(4-m-Tolyloxy-phenoxy)-propionic acid 
• 88240-24-8 1-benzoyloxy-4-m-tolyloxy-benzene 

Relevant articles and documents

Method for selectively preparing hydroquinone monoether compound or quinol compound (by machine translation)

The method comprises the following steps: taking an organic boric acid compound and a p-benzoquinone compound as a reaction raw material, under the action of a copper catalyst, selectively reacting to obtain a hydroquinone monoether compound or a quinol compound. Compared with the prior art, the method disclosed by the invention adopts a one-pot reaction, can selectively obtain two products through solvent control, is suitable for preparing various types of hydroquinone monoether compounds and quinol compounds, and has wide applicability. The substrate functional group is high in tolerance and wide in substrate range. The raw material and the catalyst are cheap and easily available, the reaction conditions are mild, the reaction solvent is green and environment-friendly, the post-treatment is simple, and the yield and purity of the product are high. The preparation method is convenient. The method is rapid and efficient, and has a good application prospect in drug molecule synthesis. (by machine translation)

Carbamic acid esters and use as pesticides

Carbamic acid compounds of the formula STR1 wherein R1, R2, R3, R4, R5, R6, X and Y are as hereinafter set forth, processes for their preparation, pesticidal compositions containing one or more of the carbamic acid compounds as the active ingredient and methods for using the pesticidal compositions for the control of pests, particularly insects, mites and nematodes, are described.