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27542-85-4

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  • 2-Propenoic acid, 3-[4-(acetyloxy)phenyl]-, (E)-

    Cas No: 27542-85-4

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27542-85-4 Usage

General Description

2-Propenoic acid, 3-[4-(acetyloxy)phenyl]-, (E)- is a chemical compound that belongs to the class of 2-propenoic acids. It is also known as 3-(4-acetoxyphenyl) acrylic acid. 2-Propenoic acid, 3-[4-(acetyloxy)phenyl]-, (E)- is characterized by its E configuration and a phenyl group, as well as an acetyloxy group attached to the phenyl ring. It has potential applications in various fields such as pharmaceuticals, polymers, and materials science. Additionally, it is important to handle this compound with care as it may have hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 27542-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,4 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27542-85:
(7*2)+(6*7)+(5*5)+(4*4)+(3*2)+(2*8)+(1*5)=124
124 % 10 = 4
So 27542-85-4 is a valid CAS Registry Number.

27542-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-acetoxyphenyl)-2-propenoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-ACETOXY-PHENYL)-ACRYLIC ACID

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:27542-85-4 SDS

27542-85-4Relevant articles and documents

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Tsujimura

, (1937)

-

Oat polyphenol avenanthramide-2c confers protection from oxidative stress by regulating the Nrf2-ARE signaling pathway in PC12 cells

Hou, Yanan,Peng, Shoujiao,Song, Zilong,Bai, Feifei,Li, Xinming,Fang, Jianguo

, (2021/05/29)

Accumulating evidence has demonstrated that cellular antioxidant systems play essential roles in retarding oxidative stress-related diseases, such as Parkinson's disease. Because nuclear factor erythroid 2-related factor 2 (Nrf2) is a chief regulator of c

Dual Nickel/Ruthenium Strategy for Photoinduced Decarboxylative Cross-Coupling of α,β-Unsaturated Carboxylic Acids with Cycloketone Oxime Esters

Gao, Ang,Jiang, Run-Chuang,Liu, Chuang-Chuang,Liu, Qi-Le,Lu, Xiao-Yu,Xia, Ze-Jie

supporting information, p. 8829 - 8842 (2021/06/30)

Herein, a dual nickel/ruthenium strategy is developed for photoinduced decarboxylative cross-coupling between α,β-unsaturated carboxylic acids and cycloketone oxime esters. The reaction mechanism is distinct from previous photoinduced decarboxylation of α,β-unsaturated carboxylic acids. This reaction might proceed through a nickelacyclopropane intermediate. The C(sp2)-C(sp3) bond constructed by the aforementioned reaction provides an efficient approach to obtaining various cyanoalkyl alkenes, which are synthetically valuable organic skeletons in organic and medicinal chemistry, under mild reaction conditions. The protocol tolerates many critical functional groups and provides a route for the modification of complex organic molecules.

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