574-13-0 Usage
Description
(E)-2-hydroxy-1,2-diphenylethan-1-one oxime, also known as benzophenone oxime, is a chemical compound characterized by its molecular formula C14H13NO. It is a versatile compound with a range of applications across different industries due to its unique properties.
Uses
Used in Polymer and Coatings Industry:
(E)-2-hydroxy-1,2-diphenylethan-1-one oxime is used as a photoinitiator for the production of polymers and coatings. Its role in this application is to facilitate the polymerization process, enabling the formation of the desired polymer or coating material.
Used in Pharmaceutical Applications:
(E)-2-hydroxy-1,2-diphenylethan-1-one oxime is being studied for its potential use in the pharmaceutical industry, particularly due to its demonstrated antioxidant properties. These properties may contribute to its effectiveness in various therapeutic applications, although further research is needed to fully understand its potential effects on human health.
Used in Cosmetic and Personal Care Products:
In the cosmetic and personal care industry, (E)-2-hydroxy-1,2-diphenylethan-1-one oxime is utilized as a UV absorber. Its ability to absorb ultraviolet radiation helps protect the skin from harmful UV rays, making it a valuable component in sunscreens and other skincare products. While it is considered relatively safe for use in these applications, ongoing research is essential to ensure its long-term safety and environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 574-13-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 574-13:
(5*5)+(4*7)+(3*4)+(2*1)+(1*3)=70
70 % 10 = 0
So 574-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO2/c16-14(12-9-5-2-6-10-12)13(15-17)11-7-3-1-4-8-11/h1-10,14,16-17H/b15-13+
574-13-0Relevant articles and documents
Readily available ruthenium complex for efficient dynamic kinetic resolution of aromatic α-hydroxy ketones
Agrawal, Santosh,Martinez-Castro, Elisa,Marcos, Rocio,Martin-Matute, Belen
, p. 2256 - 2259 (2014/05/06)
A ruthenium complex formed from commercially available [Ru(p-cymene)Cl 2]2 and 1,4-bis(diphenylphosphino)butane catalyzes the racemization of aromatic α-hydroxy ketones very efficiently at room temperature. The racemization is fully compatible with a kinetic resolution catalyzed by a lipase from Pseudomonas stutzeri. This is the first example of dynamic kinetic resolution of α-hydroxy ketones at ambient temperature in which the metal and enzyme catalysts work in concert in one pot at room temperature to give quantitative yields of esters of α-hydroxy ketones with very high enantioselectivity.
Lipase TL-mediated kinetic resolution of benzoin: Facile synthesis of (1R,2S)-erythro-2-amino-1,2-diphenylethanol
Aoyagi, Yutaka,Agata, Naoki,Shibata, Noriko,Horiguchi, Mai,Williams, Robert M.
, p. 10159 - 10162 (2007/10/03)
The lipase TL-mediated kinetic resolution of (±)-benzoin (1) proceeded to give the corresponding optically pure benzoin (R)-1. On the other hand, (S)-benzoin-O-acetate (5) could be hydrolyzed without epimerization to give (S)-benzoin (S)-1, under alkaline conditions. Further, (R)-1 was converted to (1R,2S)-2-amino-1,2-diphenylethanol (99:1 er) according to the procedure reported previously. (C) 2000 Elsevier Science Ltd.
Asymmetric Synthesis of the Methyl and Benzyl Ethers of erythro-α,β-Diphenyl-β-hydroxyethanol and erythro-α,β-Diphenyl-β-hydroxyethylamine from (+)-(S)-Benzoin
Davis, Franklin A.,Haque, M. S.,Przeslawski, Robert M.
, p. 2021 - 2024 (2007/10/02)
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