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7465-91-0

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7465-91-0 Usage

General Description

4-Ethylphenyl 4-methoxybenzoate is a chemical compound with the molecular formula C17H16O3. It is a derivative of benzoic acid and belongs to the group of aromatic esters. This chemical is commonly used in the manufacturing of personal care products, such as sunscreens and skincare lotions, due to its UV absorption properties. It acts as a UV filter, protecting the skin from harmful radiation. Additionally, it is also used in the production of fragrances and as a flavoring agent in the food industry. 4-Ethylphenyl 4-methoxybenzoate has potential applications in pharmaceuticals and textile industries as well.

Check Digit Verification of cas no

The CAS Registry Mumber 7465-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7465-91:
(6*7)+(5*4)+(4*6)+(3*5)+(2*9)+(1*1)=120
120 % 10 = 0
So 7465-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O3/c1-3-12-4-8-15(9-5-12)19-16(17)13-6-10-14(18-2)11-7-13/h4-11H,3H2,1-2H3

7465-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-ethylphenyl) 4-methoxybenzoate

1.2 Other means of identification

Product number -
Other names 4-Ethylphenyl 4-methoxybenzoate

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:7465-91-0 SDS

7465-91-0Downstream Products

7465-91-0Relevant articles and documents

N-heterocyclic carbene-catalyzed aerobic oxidative direct esterification of aldehydes with organoboronic acids

Meng, Jing-Jing,Gao, Min,Wei, Yu-Ping,Zhang, Wen-Qin

experimental part, p. 872 - 875 (2012/07/03)

A simple procedure affording benzoates through a NHC-catalyzed aerobic oxidative esterification of aldehydes with organoboronic acids has been disclosed. This process allows access to a wide variety of aromatic esters in good to excellent yields under simple, efficient, and sustainable reaction conditions (see scheme).

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