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Butanedioic acid, 2-propenyl, dimethyl ester, also known as dimethyl allylsuccinate, is a colorless liquid organic compound with the chemical formula C8H12O4. It is a derivative of butanedioic acid (succinic acid), where the hydrogen atoms are replaced by an allyl group (2-propenyl) and two methyl groups. This ester is used as a monomer in the production of polymers, particularly in the synthesis of polyaspartic acid, which has applications in various industries such as coatings, adhesives, and water treatment. It is also employed as a chemical intermediate in the synthesis of other compounds. Due to its reactivity, it is important to handle Butanedioic acid, 2-propenyl-, dimethyl ester with care, following proper safety protocols.

1069-40-5

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1069-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1069-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1069-40:
(6*1)+(5*0)+(4*6)+(3*9)+(2*4)+(1*0)=65
65 % 10 = 5
So 1069-40-5 is a valid CAS Registry Number.

1069-40-5SDS

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 dimethyl 2-allylsuccinate

1.2 Other means of identification

Product number -
Other names dimethyl 2-(prop-2-en-1-yl)butanedioate

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:1069-40-5 SDS

1069-40-5Downstream Products

1069-40-5Relevant academic research and scientific papers

Electrochemical Coupling of Activated Olefins and Alkyl Dihalides: Formation of Cyclic Compounds

Lu, Yu-Wei,Nedelec, Jean-Yves,Folest, Jean-Claude,Perichon, Jacques

, p. 2503 - 2507 (1990)

The electrochemical coupling of dimethyl maleate, methyl cinnamate, 4-phenyl-3-buten-2-one, or methyl acrylate with dibromomethane, 1,3-dibromopropane, 1,4-dibromobutane or other substituted alkyl dihalogenides gave satisfactory yields of cyclic products.The reactions were performed in an undivided cell fitted with a sacrificial aluminum anode, in N-methylpyrrolidone (NMP), at constant current, and at room temperature.The role of the anodically generated metallic ions in this cyclocondensation has been evidenced.

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