10534-77-7 Usage
Uses
Used in Polymer Production:
(Z)-2-Butenedioic acid bis(2-phenoxyethyl) ester is used as a plasticizer for the production of polymers, particularly in the manufacture of vinyl, neoprene, and other synthetic rubber materials. It enhances the flexibility and workability of these materials.
Used in Resin Solvent:
(Z)-2-Butenedioic acid bis(2-phenoxyethyl) ester is used as a solvent for resins, helping to dissolve and mix them effectively for various applications.
Used in Organic Synthesis:
(Z)-2-Butenedioic acid bis(2-phenoxyethyl) ester is used as an intermediate in the synthesis of various organic compounds, contributing to the creation of new chemical entities for different industries.
Safety:
This chemical has low toxicity and is not known to be carcinogenic, mutagenic, or teratogenic. However, it should be handled with caution and in accordance with proper safety measures to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 10534-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,3 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10534-77:
(7*1)+(6*0)+(5*5)+(4*3)+(3*4)+(2*7)+(1*7)=77
77 % 10 = 7
So 10534-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O6/c21-19(25-15-13-23-17-7-3-1-4-8-17)11-12-20(22)26-16-14-24-18-9-5-2-6-10-18/h1-12H,13-16H2/b12-11-
10534-77-7Relevant academic research and scientific papers
Photoorganocatalytic synthesis of lactones: Via a selective C-H activation-alkylation of alcohols
Kaplaneris, Nikolaos,Bisticha, Aikaterini,Papadopoulos, Giorgos N.,Limnios, Dimitris,Kokotos, Christoforos G.
supporting information, p. 4451 - 4456 (2017/09/29)
Selective C-H activation is an area of growing importance in modern organic chemistry. Herein, we report our efforts in combining organocatalysis and photocatalysis for the development of a highly efficient and selective visible-light mediated protocol for the C-H activation and addition of various alcohols to a plethora of Michael acceptors, followed by a cyclization reaction leading to lactones, a repeatedly occurring motif in nature. Utilizing phenylglyoxylic acid as the photocatalyst and common household bulbs as the light source, we describe a versatile α-alkylation/lactonization of alcohols with α,β-unsaturated esters leading to products in excellent yields. The reaction mechanism was extensively studied.
