73584-59-5 Usage
General Description
1-(1-Hydroxy-4-Methoxy-Naphthalen-2-Yl)-Ethanone is a chemical compound with a molecular formula of C13H12O3. It is a derivative of naphthalene and is commonly used in organic synthesis and medicinal chemistry. 1-(1-HYDROXY-4-METHOXY-NAPHTHALEN-2-YL)-ETHANONE is known for its aromatic properties and is often used as a reagent in the production of various pharmaceuticals and agrochemicals. It is also used as a building block in the manufacture of dyes and pigments. Additionally, it has been studied for its potential antioxidant and anti-inflammatory properties. Overall, 1-(1-Hydroxy-4-Methoxy-Naphthalen-2-Yl)-Ethanone is a versatile and important compound with a wide range of applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 73584-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,8 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73584-59:
(7*7)+(6*3)+(5*5)+(4*8)+(3*4)+(2*5)+(1*9)=155
155 % 10 = 5
So 73584-59-5 is a valid CAS Registry Number.
73584-59-5Relevant articles and documents
The Catalytic Fries Rearrangement and o-Acylation Reactions Using Group 3 and 4 Metal Triflates as Catalysts
Kobayashi, Shue,Moriwaki, Mitsuhiro,Hachiya, Iwao
, p. 267 - 273 (2007/10/03)
Group 3 and 4 metal triflates (Sc(OTf)3, TiCl(OTf)3, Zr(OTf)4, and Hf(OTf)4) were found to be efficient catalysts in the Fries rearrangement of phenyl or 1 -naphthyl acylates. It was also found that the o-acylation (direct acylation) reactions of phenols and 1-naphthols with acid chlorides proceeded smoothly in the presence of the triflates. Both reactions were successfully carried out using small amounts of the triflates (catalytically), and comparison of catalytic activities of these metal triflates in these reactions is discussed.
