32852-93-0

Usage

Uses

Used in Fragrance Industry:
1-(3-phenoxyphenyl)ethanol is used as a fragrance ingredient for its floral and fruity scent, enhancing the appeal of cosmetics, personal care products, and household cleaning products.
Used in Chemical Synthesis:
1-(3-phenoxyphenyl)ethanol serves as an intermediate in the synthesis of various organic compounds, including pharmaceuticals, pesticides, and industrial chemicals, contributing to the development of a wide range of products.
Used in Cosmetics and Personal Care Products:
1-(3-phenoxyphenyl)ethanol is used as a fragrance ingredient in the cosmetics and personal care industry to provide a pleasant scent and enhance the overall sensory experience of the products.
Used in Household Cleaning Products:
In the household cleaning products industry, 1-(3-phenoxyphenyl)ethanol is used to add a fresh and appealing scent, making the cleaning experience more enjoyable for consumers.
Safety:
1-(3-phenoxyphenyl)ethanol is considered a relatively safe chemical with low acute toxicity. However, it is important to note that prolonged or high-level exposure may cause irritation to the skin, eyes, and respiratory system. As a result, proper handling and usage guidelines should be followed to ensure safety.

Upstream product

• 32852-92-9 3'-phenoxyacetophenone 
• 75-16-1 methylmagnesium bromide 
• 39515-51-0 3-Phenoxybenzaldehyde 
• 108-95-2 phenol 
• 2142-63-4 1-(3-Bromophenyl)ethanone 

Downstream Products

• 32852-94-1 m-phenoxy-α-methylbenzyl bromide 
• 32929-71-8 2-(3-Phenoxy-phenyl)-propylamine 
• 32852-95-2 alpha-(m-phenoxyphenyl)propionitrile 
• 32949-88-5 1-Methyl-3-[2-(3-phenoxy-phenyl)-propyl]-urea 
• 32953-79-0 2-(3-Phenoxy-phenyl)-propionic acid 
• 32953-79-0 2-(3-Phenoxy-phenyl)-propionic acid 
• 64628-80-4 α-methyl-m-phenoxybenzyl 2-(2',2'-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylate 
• 80379-89-1 1-(m-phenoxyphenyl)-1-chloroethane 

Relevant academic research and scientific papers

A new convenient reduction of aralkyl ketones to alcohols using Raney nickel-ammonium formate

Various aralkyl ketones have been reduced to their corresponding alcohols in high yield using Raney Ni-HCO2NH4.

Nickel-Catalyzed Stereo- and Enantioselective Cross-Coupling of gem-Difluoroalkenes with Carbon Electrophiles by C?F Bond Activation

Stereo- and enantioselective cross-electrophile coupling involving C?F bond activation is reported. Treatment of gem-difluoroalkenes with racemic benzyl electrophiles in the presence of a chiral nickel complex using B2pin2 as a stoichiometric reductant allows the construction of a C(sp2)?C(sp3) bond under mild conditions, affording a broad range of monofluoroalkenes bearing stereogenic allylic centers. Initial mechanistic studies indicate that a radical chain pathway may be operating, wherein the ester group in the gem-difluoroalkene promotes C?F bond activation through oxidative addition to a Ni species.

Novel method for high-yield preparation of roxadustat intermediate

The invention discloses a preparation method of a roxadustat intermediate. The preparation method comprises the following steps: (1) subjecting a compound 1 and a compound 2 to reacting in an organic solvent under the catalysis of alkali to obtain an intermediate 3; (2) reducing the intermediate 3 in an organic solvent through a reducing agent to obtain an intermediate 4; (3) subjecting the intermediate 4 to reacting with a bromination reagent in an organic solvent to obtain an intermediate 5; (4) subjecting the intermediate 5 to reacting with a compound 6 in an organic solvent under the catalysis of acid to obtain an intermediate 7; (5) carrying out a cyclization reaction on the intermediate 7 in an organic solvent and a catalytic system to prepare an intermediate 8; and (6) subjecting the intermediate 8 to reacting in an organic solvent through a dehydrogenation reagent to obtain the roxadustat intermediate 9. The preparation method of the roxadustat intermediate has the advantages that raw materials are easy to obtain, operation steps are few, a process is simple, reaction yield is high, an atom utilization rate is high, and industrial production is easy.

RECEPTOR FUNCTION REGULATING AGENT

An agent for regulating 14273 receptor function, which is useful as a preventing or treating drug for diabetes mellitus, hyperlipidemia or the like, is provided. An agent for regulating 14273 receptor function comprising a compound containing an aromatic ring and a group capable of releasing a cation.