33926-25-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Organic Synthesis as a Reactant:
In organic synthesis, ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE serves as a reactant for the production of esters, facilitating the formation of diverse organic compounds.
Used as a Protecting Group in Organic Synthesis:
ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE can be utilized as a protecting group in organic synthesis, helping to shield functional groups during chemical reactions and ensuring the desired product formation.
Used in Organic Electronics:
With its potential applications in the field of organic electronics, ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE can contribute to the development of advanced electronic devices and materials.
Used as a Photoinitiator in Photopolymerization Reactions:
ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE has the potential to be used as a photoinitiator in photopolymerization reactions, enabling the rapid and efficient formation of polymers under light exposure.
It is essential to handle and use ETHYL 4-(4'-ETHOXYPHENOXYCARBONYL)PHENYL CARBONATE with proper safety precautions and guidelines to ensure safe and effective applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 33926-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,2 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33926-25:
(7*3)+(6*3)+(5*9)+(4*2)+(3*6)+(2*2)+(1*5)=119
119 % 10 = 9
So 33926-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O6/c1-3-21-14-9-11-15(12-10-14)23-17(19)13-5-7-16(8-6-13)24-18(20)22-4-2/h5-12H,3-4H2,1-2H3
33926-25-9Relevant articles and documents
Liquid crystals V.Nematic materials derived from p- alkylcarbonato- p- alkoxyphenyl benzoates
CASTELLANO JA,MCCAFFREY MT,GOLDMACHER JE
, p. 345 - 366 (2007/10/14)
In a continued effort to synthesize materials which exhibit nematic behavior at room temperature, homologous p- alkylcarbonato- p- alkoxyphenyl benzoates were prepared. Of the 48 compounds that were synthesized 27 exhibited enantiotropic and 14 manotropic nematic properties while only 7 were not liquid crystalline. One binary mixture of anantiotropic derivatives had a nematic range of 27 to 73 C while a ternary mixture exhibited nematic behavior between 24 and 76 C. In addition, seven other mixtures had crystal to nematic transition temperatures below 30 C.
