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2-Propenoic acid, 3-(3,4-dioxo-1,5-cyclohexadien-1-yl)-, methyl ester, also known as methyl 3-(3,4-dioxo-1,5-cyclohexadien-1-yl)acrylate, is a complex organic compound with the chemical formula C10H8O4. It is a derivative of acrylic acid, featuring a cyclohexadienyl group attached to the acrylic acid backbone. 2-Propenoic acid, 3-(3,4-dioxo-1,5-cyclohexadien-1-yl)-, methyl ester is characterized by its conjugated double bonds and the presence of a methyl ester group, which contributes to its reactivity and potential applications in various chemical processes. It is often used in the synthesis of polymers and other organic compounds due to its reactive nature and ability to participate in addition reactions. The compound's structure and properties make it a valuable intermediate in the chemical industry, particularly in the production of specialty polymers and resins.

1782-53-2

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1782-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1782-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1782-53:
(6*1)+(5*7)+(4*8)+(3*2)+(2*5)+(1*3)=92
92 % 10 = 2
So 1782-53-2 is a valid CAS Registry Number.

1782-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(3,4-dioxocyclohexa-1,5-dien-1-yl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names -

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:1782-53-2 SDS

1782-53-2Downstream Products

1782-53-2Relevant academic research and scientific papers

Antioxidation mechanism studies of caffeic acid: Identification of antioxidation products of methyl caffeate from lipid oxidation

Masuda, Toshiya,Yamada, Kazuki,Akiyama, Jun,Someya, Tatsushi,Odaka, Yuka,Takeda, Yoshio,Tori, Motoo,Nakashima, Katsuyuki,Maekawa, Tomomi,Sone, Yoshiaki

, p. 5947 - 5952 (2008)

As a part of a research project on the elucidation of the chain-breaking antioxidation mechanism of natural phenols in food components, caffeic acid, a polyphenolic acid widely distributed in edible plants, was investigated. The identification and time course analysis of the antioxidation reaction products from methyl caffeate were carried out in the ethyl linoleate oxidation system. The antioxidation reaction produced a quinone derivative of methyl caffeate as an antioxidation product during the initial stage, which was identified by 13C NMR. The quinone, however, was not the final product, and a further reaction occurred to produce several new peroxides. The isolation and structure determination of the peroxides revealed that they had tricyclic structures, which consisted of ethyl linoleate, methyl caffeate, and molecular oxygen. On the basis of the formation pathway of these products, an antioxidation reaction mechanism of methyl caffeate, including the redox reaction of the caffeate and Diels-Alder reaction of the produced peroxides, was proposed.

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