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Acrylic acid methyl ester, also known as methyl acrylate or acetylacrylic acid methyl ester, is a colorless liquid with the chemical formula C4H6O2. It is an ester derived from acrylic acid and methanol, and is widely used in the production of polymers, resins, and adhesives. This chemical is also employed as a comonomer in the synthesis of various copolymers, such as polymethyl methacrylate (PMMA), which is commonly known as acrylic glass or Plexiglas. Methyl acrylate is a highly reactive compound and is considered hazardous due to its potential to cause respiratory and skin irritation, as well as its flammability and explosive properties. It is important to handle this chemical with proper safety measures and in accordance with established guidelines.

2833-24-1

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2833-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2833-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2833-24:
(6*2)+(5*8)+(4*3)+(3*3)+(2*2)+(1*4)=81
81 % 10 = 1
So 2833-24-1 is a valid CAS Registry Number.

2833-24-1SDS

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 ACETYLACRYLIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names methyl trans-4-oxo-2-pentanoate

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:2833-24-1 SDS

2833-24-1Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF ALKYL 5- (DICARBOXIMIDO) LEVULINATE AND ALKYL 4-OXO-PENTENOATE

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Page/Page column 6-7, (2008/06/13)

A method of manufacturing esters of dicarboxyimidolevulinic acid and alkyl trans-4-oxo-2-pentenoate. This method includes two reaction steps, wherein the first step of said two reaction steps is a bromination of alkyl-levulinate, to obtain alkyl-(3 and 5)-bromolevulinate, and the second step of said two reaction steps is a synthesis of esters of dicarboxyimidolevulinic acid and alkyl trans-4-oxo-2-pentenoate, by reacting the alkyl-(3 and 5)-bromolevulinate obtained in said first step with dicarboxyimide anion.

A Flexible and Efficient Synthesis of Methyl 4-Oxo-2-alkenoates

Reichelt, Ingrid,Reissig, Hans-Ulrich

, p. 820 - 827 (2007/10/02)

The title compounds E are obtained in good yield by low temperature ring cleavage of the easily available methyl 2-siloxycyclopropanecarboxylates C with bromine and subsequent elimination of hydrogen bromide.Due to the variability of C a high flexibility concerning substituents R1 - R4 in products E is guaranteed. 2-Alkyl- and 2-methylthio-substituted olefins are thus effectively synthesized.In several cases the initially formed methyl 2-bromo-4-oxoalkanoates F are stable enough to be isolated in high yield.

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