73584-59-5 Usage
Uses
Used in Pharmaceutical Industry:
1-(1-Hydroxy-4-Methoxy-Naphthalen-2-Yl)-Ethanone is used as a reagent for the synthesis of various pharmaceuticals due to its aromatic properties and ability to contribute to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1-HYDROXY-4-METHOXY-NAPHTHALEN-2-YL)-ETHANONE is utilized as a reagent in the production of agrochemicals, contributing to the development of effective and safe products for agricultural applications.
Used in Dye and Pigment Manufacturing:
1-(1-Hydroxy-4-Methoxy-Naphthalen-2-Yl)-Ethanone serves as a building block in the manufacture of dyes and pigments, providing a foundation for the creation of a wide range of colorants used in various industries.
Used in Organic Synthesis:
As a versatile compound, 1-(1-HYDROXY-4-METHOXY-NAPHTHALEN-2-YL)-ETHANONE is used in organic synthesis for the development of new chemical compounds and materials.
Used in Research and Development:
1-(1-Hydroxy-4-Methoxy-Naphthalen-2-Yl)-Ethanone is employed in research and development for studying its potential antioxidant and anti-inflammatory properties, which could lead to the discovery of new applications in medicine and other fields.
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 academic research and scientific papers
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.
Approach to the Synthesis of Bridgehead Substituted Furo[3,2-b]furans and Side Products of McMurry Reactions
Laatsch, Hartmut,Talvitie, Antti,Kral, Andreas,Ernst, Bernd-Peter,Noltemeyer, Mathias
, p. 140 - 145 (2007/10/02)
Substituted dihydroxystilbenes 2 are suitable starting materials for the synthesis of photochromic systems derived from 3/4. Attempts to couple the naphthones 8a-8e by the McMurry reaction with TiCl3/LiAlH4 yielded mainly reduction products such as 8f, g or 9. However, the furofuran 3b was isolated when using the zinc-copper couple for reduction. The helicene 11 was formed as an unexpected by-product in the McMurry reaction of the pivaloylnaphthalene 8d.
