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32852-93-0

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32852-93-0 Usage

Description

1-(3-phenoxyphenyl)ethanol, with the molecular formula C14H14O2, is a chemical compound that is colorless to pale yellow in appearance and has a slightly sweet odor. It is recognized for its pleasant floral and fruity scent, making it a popular choice as a fragrance ingredient in various industries.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 32852-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,5 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32852-93:
(7*3)+(6*2)+(5*8)+(4*5)+(3*2)+(2*9)+(1*3)=120
120 % 10 = 0
So 32852-93-0 is a valid CAS Registry Number.

32852-93-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (RS)-1-(3-phenoxyphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(3-phenoxyphenyl)ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32852-93-0 SDS

32852-93-0Relevant articles and documents

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

Chen,Zhang,Yuan,Zhang

, p. 107 - 109 (1991)

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

Novel method for high-yield preparation of roxadustat intermediate

-

Paragraph 0046-0049, (2021/08/14)

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.

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