42529-03-3 Usage
Description
4-(2-Acetoxyacetyl)-1,2-phenylene diacetate is a chemical compound with the formula C14H14O7. It is an ester formed from the reaction between 4-hydroxybenzophenone and acetoacetic acid. 4-(2-Acetoxyacetyl)-1,2-phenylene diacetate serves as a building block in the synthesis of more complex organic compounds and has potential uses in various fields, including pharmaceuticals, polymers, and other materials. Due to its potential hazardous properties, it is crucial to handle this compound with care and adhere to safe laboratory practices and regulations.
Uses
Used in Pharmaceutical Industry:
4-(2-Acetoxyacetyl)-1,2-phenylene diacetate is used as a building block for the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Polymer Industry:
In the polymer industry, 4-(2-Acetoxyacetyl)-1,2-phenylene diacetate is used as a monomer or intermediate in the production of polymers with specific properties. Its incorporation into polymer chains can lead to materials with enhanced characteristics for various applications.
Used in Research Applications:
4-(2-Acetoxyacetyl)-1,2-phenylene diacetate is utilized in research settings for the development and study of new organic compounds and materials. Its reactivity and structural features make it a valuable tool for exploring novel chemical reactions and syntheses.
Used in Material Science:
In material science, 4-(2-Acetoxyacetyl)-1,2-phenylene diacetate is employed in the synthesis of advanced materials with tailored properties. Its potential use in creating new materials with improved performance can contribute to the development of innovative products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 42529-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42529-03:
(7*4)+(6*2)+(5*5)+(4*2)+(3*9)+(2*0)+(1*3)=103
103 % 10 = 3
So 42529-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O7/c1-8(15)19-7-12(18)11-4-5-13(20-9(2)16)14(6-11)21-10(3)17/h4-6H,7H2,1-3H3
42529-03-3Relevant articles and documents
Effect of Methyl, Hydroxyl, and Chloro Substituents in Position 3 of 3′,4′,7-Trihydroxyflavylium: Stability, Kinetics, and Thermodynamics
Alejo-Armijo, Alfonso,Salido, Sofía,Altarejos, Joaquín,Parola, A. Jorge,Gago, Sandra,Basílio, Nuno,Cabrita, Luis,Pina, Fernando
, p. 12495 - 12505 (2016)
The effect of methyl, hydroxyl, and chloride substituents in position 3 of the 3′,4′,7-trihydroxyflavylium core structure was studied. The stability, relative energy of each of chemical species (thermodynamics), and their rates of interconversion (kinetics) are very dependent on these substituents. By comparing the mole fraction distribution at equilibrium of the three multistate systems with the parent 3′,4′,7-trihydroxyflavylium, introduction of a methyl substituent in position 3 increases the mole fraction of hemiketal at the expense of the trans-chalcone and increases the hydration rate very significantly; a hydroxyl substituent in position 3 gives rise to a degradation process, as observed in anthocyanidins. In the case of 3-chloro-3′,4′,7-trihydroxyflavylium, a dramatic increase of the flavylium cation acidity was observed and a photochromic system can be operated upon irradiation of the respective trans-chalcone in 1 m HCl. According to the photochromic response of 3,3′,4′,7-tetrahydroxyflavylium and 3′,4′,7-trihydroxyflavylium, some requirements for a good photochromic performance are discussed.
