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1,3-Benzenedicarboxylic acid, diethenyl ester, also known as phthalic acid diethyl ester, is an organic compound with the chemical formula C12H14O4. It is a colorless, oily liquid that is soluble in most organic solvents. This ester is formed by the reaction of phthalic acid with ethanol in the presence of a catalyst, typically an acid catalyst like sulfuric acid. It is used as a solvent and a chemical intermediate in the production of various chemicals, including plasticizers, dyes, and resins. It is also used in the synthesis of certain pharmaceuticals and as a reagent in organic chemistry. Due to its potential health risks, it is important to handle 1,3-Benzenedicarboxylic acid, diethenyl ester with care, following proper safety protocols.

20778-88-5

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20778-88-5 Usage

Physical state

Colorless, odorless liquid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Solvent in various industries
b. Plasticizer to add flexibility and durability to plastic products
c. Ingredient in cosmetics, detergents, and personal care products
d. Solvent for dyes
e. Fixative for perfumes

Health concerns

Potential health hazards have led to restrictions on its use in some countries

Check Digit Verification of cas no

The CAS Registry Mumber 20778-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,7 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20778-88:
(7*2)+(6*0)+(5*7)+(4*7)+(3*8)+(2*8)+(1*8)=125
125 % 10 = 5
So 20778-88-5 is a valid CAS Registry Number.

20778-88-5Downstream Products

20778-88-5Relevant academic research and scientific papers

Novel synthesis routes for the preparation of low toxic vinyl ester and vinyl carbonate monomers

Hofecker, Andreas,Knaack, Patrick,Liska, Robert,Markovic, Marica,Ovsianikov, Aleksandr,Steinbauer, Patrick

supporting information, p. 3629 - 3641 (2020/10/02)

UV curing of photopolymerizable monomers, like (meth)acrylates, has been utilized for coatings for more than half a century and more recently in further developed areas such as tissue engineering. However, these monomers have major disadvantages, e.g., high irritancy and cytotoxicity, which leads to limited use in tissue engineering regarding health issues. Vinyl esters (VE) and vinyl carbonates (VC) can compete with (meth)acrylates in terms of material properties and have significantly lower toxicity, but lack in cost efficient synthesis methods. The purpose of this communication is to establish new pathways to overcome this drawback. It was shown that VEs can be synthesized either by vinyloxy trimethylsilane or by acetaldehyde in excellent yields. Moreover, a new method to synthesize vinyl chloroformate as precursor for VCs in lab scale was evolved by a catalyzed reaction of vinyloxy trimethylsilane with a phosgene solution. Finally, the cytotoxicity tests showed auspicious results.

Transvinylation process for the preparation of thermally labile vinyl compounds and for vinyl compounds prepared from thermally labile acids

-

, (2008/06/13)

A process for the transvinylation of a vinyl derivative of a Bronsted acid with a different Bronsted acid which comprises providing a liquid phase mixture containing said vinyl derivative and said Bronsted acid in the presence of a ruthenium compound at a temperature at which transvinylation occurs and recovering as a product of transvinylation the vinyl derivative of the different Bronsted acid. The process is most favorably employed using carboxylic acids to make vinyl esters of carboxylic acids.

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