1026-92-2 Usage
Description
TEREPHTHALIC ACID DIALLYL ESTER, commonly known as Diallyl Terephthalate (DAT), is a synthetic organic compound derived from terephthalic acid and allyl alcohol. It is characterized by its clear, colorless, and viscous liquid properties. The molecular structure of DAT consists of a terephthalic acid core with two allyl ester groups attached, which contributes to its unique chemical and physical properties.
Uses
Used in Plasticizer Industry:
TEREPHTHALIC ACID DIALLYL ESTER is used as a plasticizer for [application reason] to enhance the flexibility, workability, and processability of various polymers, particularly in the production of polyvinyl chloride (PVC) products. Its compatibility with PVC and its ability to improve the material's properties make it a valuable additive in the plasticizer industry.
Used in Organotin Polymers Preparation:
TEREPHTHALIC ACID DIALLYL ESTER is used as a key component in the preparation of organotin polymers for [application reason] to create materials with unique properties, such as improved thermal stability, flame retardancy, and mechanical strength. These organotin polymers find applications in various industries, including electronics, automotive, and aerospace, where high-performance materials are required.
Check Digit Verification of cas no
The CAS Registry Mumber 1026-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1026-92:
(6*1)+(5*0)+(4*2)+(3*6)+(2*9)+(1*2)=52
52 % 10 = 2
So 1026-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O4/c1-3-9-17-13(15)11-5-7-12(8-6-11)14(16)18-10-4-2/h3-8H,1-2,9-10H2
1026-92-2Relevant articles and documents
Efficient synthesis of macrocyclic paracyclophanes by ring-closing metathesis dimerization and trimerization reactions
Tae, Jinsung,Yang, Young-Keun
, p. 741 - 744 (2007/10/03)
(Matrix presented) Ring-closing metathesis reactions of para-disubstituted aromatic substrates produced macrocyclic [n.n]-, and [n.n.n]paracyclophanes efficiently through dimerization and trimerization reactions. Sufficiently long alkyl chains allowed direct monocyclizations to yield [n]paracyclophanes. A small library of paracyclophanes were generated by the combinatorial cross-metathesis approach.
Solid-Liquid Phase-Transfer Catalysis without Added Solvent. A Simple, Efficient, and Inexpensive Synthesis of Aromatic Carboxylic Esters by Alkylation of Potassium Carboxylates
Barry, J.,Bram, G.,Decodts, G.,Loupy, A.,Orange, C.,et al.
, p. 40 - 45 (2007/10/02)
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