57267-03-5 Usage
Uses
Used in Coatings Industry:
Acetic acid, triethoxy-, ethyl ester is used as a solvent for the production of lacquers, varnishes, and other coatings, providing a smooth finish and enhancing the application process.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, acetic acid, triethoxy-, ethyl ester is utilized as a solvent in the manufacturing process, aiding in the dissolution and stability of various medicinal compounds.
Used in Food Industry:
As a flavoring agent, acetic acid, triethoxy-, ethyl ester is employed in the food industry to impart specific tastes and scents to food products, enhancing their overall appeal.
Safety and Handling:
Due to its flammable nature and potential hazards, acetic acid, triethoxy-, ethyl ester requires careful handling and storage. It should be used in well-ventilated areas, and appropriate personal protective equipment should be worn to prevent inhalation, ingestion, or skin absorption. Regulatory compliance and safety precautions are essential to mitigate health and environmental risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 57267-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,6 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57267-03:
(7*5)+(6*7)+(5*2)+(4*6)+(3*7)+(2*0)+(1*3)=135
135 % 10 = 5
So 57267-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O5/c1-5-12-9(11)10(13-6-2,14-7-3)15-8-4/h5-8H2,1-4H3
57267-03-5Relevant articles and documents
Facile synthesis of 2,6-disubstituted benzobisthiazoles: Functional monomers for the design of organic semiconductors
Mike, Jared F.,Inteman, Jeremy J.,Ellern, Arkady,Jeffries-EL, Malika
supporting information; scheme or table, p. 495 - 497 (2010/03/25)
(Chemical Equation Presented) The synthesis of several synthetically useful 2,6-disubstituted benzobisthiazoles is described. The method is based on the Lewis acid-catalyzed ring-closing reaction between substituted orthoesters and diamino benzene dithiol. The resulting benzobisthiazoles are obtained cleanly and in good yields. These materials are of interest for the development of new organic semiconductors.
