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38495-73-7

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38495-73-7 Usage

General Description

1-(4-ethoxyphenyl)-2-phenylethanone, also known as ethyl 4-ethoxyphenyl phenylacetate, is a chemical compound with the molecular formula C17H18O2. It is a pale yellow, oily liquid with a floral and fruity odor. 1-(4-ethoxyphenyl)-2-phenylethanone is commonly used in the production of fragrances and flavors due to its pleasant scent. It is also utilized as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Additionally, 1-(4-ethoxyphenyl)-2-phenylethanone is known for its potential antimicrobial, antioxidant, and antiviral properties, making it a valuable ingredient in the development of various healthcare products. Overall, this chemical compound has a wide range of applications in the fragrance, flavor, pharmaceutical, and healthcare industries.

Check Digit Verification of cas no

The CAS Registry Mumber 38495-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38495-73:
(7*3)+(6*8)+(5*4)+(4*9)+(3*5)+(2*7)+(1*3)=157
157 % 10 = 7
So 38495-73-7 is a valid CAS Registry Number.

38495-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-ethoxyphenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names p-Ethoxy-phenyl-benzyl-keton

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:38495-73-7 SDS

38495-73-7Relevant articles and documents

Catalyst-controlled highly selective coupling and oxygenation of olefins: A direct approach to alcohols, ketones, and diketones

Su, Yijin,Sun, Xiang,Wu, Guolin,Jiao, Ning

supporting information, p. 9808 - 9812 (2013/09/23)

Oxygen? That's radical! A method for the direct synthesis of substituted alcohols, ketones, and diketones through a catalyst-controlled highly chemoselective coupling and oxygenation of olefins has been developed. The method is simple and practical, can be switched by the selection of different catalysts, and employs molecular oxygen as both an oxidant and a reagent. Copyright

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