58282-50-1 Usage
Description
5-Acetyloxyethyl-2-hydroxypheny Ethanone is an organic compound with the chemical formula C10H10O3. It is a yellow oil at room temperature and is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
5-Acetyloxyethyl-2-hydroxypheny Ethanone is used as a key intermediate compound for the preparation of benzopyran derivatives, which possess anti-inflammatory properties. These derivatives can be further utilized in the development of medications targeting inflammation-related conditions, making it a valuable component in the pharmaceutical sector.
Used in Chemical Synthesis:
As a versatile organic compound, 5-Acetyloxyethyl-2-hydroxypheny Ethanone can be employed in various chemical synthesis processes. Its unique structure allows it to be a building block for the creation of more complex molecules with potential applications in different industries, such as materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
Due to its unique chemical properties and potential applications, 5-Acetyloxyethyl-2-hydroxypheny Ethanone can be used in research and development for exploring new chemical reactions, synthesis methods, and potential applications in various fields. This can lead to the discovery of new compounds and materials with improved properties and functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 58282-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58282-50:
(7*5)+(6*8)+(5*2)+(4*8)+(3*2)+(2*5)+(1*0)=141
141 % 10 = 1
So 58282-50-1 is a valid CAS Registry Number.
58282-50-1Relevant articles and documents
Red/near-infrared light-emitting organic-inorganic hybrids doped with covalently bound boron dipyrromethene (BODIPY) dyes via microwave-assisted one-pot process
Kajiwara, Yuichi,Nagai, Atsushi,Chujo, Yoshiki
experimental part, p. 471 - 481 (2011/07/09)
Red/near-infrared (NIR) light-emitting boron dipyrromethene (BODIPY) dyes bearing methacryloyl groups were synthesized, and these dyes were covalently bonded to poly(2-hydroxyethyl methacrylate) (PHEMA)silica hybrids. The preparation of their hybrids was performed by simultaneous solgel reaction of trimethoxy(methyl)silane and radical copolymerization of 2-hydroxyethyl methacrylate (HEMA) with the dyes under microwave irradiation or conventional heating. Strong red/NIR light-emitting hybrids without discoloration of the dyes were successfully obtained under microwave irradiation, whereas the dyes lost luminescent properties in the hybrids prepared under conventional heating. Photostability test of the hybrids showed that covalent attachment of the dyes led to significant improvement in the photostability in comparison with the solution state. Further, elution amount of the dyes from the hybrids in organic solvents decreased relative to that from physical dye-admixing hybrids due to the covalent bond between PHEMA and the dyes.
Method of treating inflammation with 2-(2,3-dihydro-2-isopropyl-4-oxo-4H-1-benzopyran-6-yl)propionic acid
-
, (2008/06/13)
There are described compounds of formula I, STR1 in which Ra is hydrogen, alkyl, alkenyl or phenyl, R3, r5, r7 and R8, which may be the same or different, are each hydrogen, alkyl, alkoxy, halogen, hydroxy, alke
