40420-48-2 Usage
Uses
Used in Fragrance Industry:
1-(1,4-dihydroxynaphthalen-2-yl)ethanone is used as a perfuming agent for its distinct and strong odor, adding a pleasant scent to various products in the fragrance industry.
Used in Cosmetics and Personal Care Products:
Diosone is used as an ingredient in cosmetics and personal care products, where it contributes to the overall fragrance and sensory experience of these products.
Used in Flavoring Agents:
1-(1,4-dihydroxynaphthalen-2-yl)ethanone is also utilized in the production of flavoring agents, enhancing the taste and aroma of various consumable products.
Used in Organic Synthesis and Pharmaceuticals:
Diosone serves as an intermediate in organic synthesis and pharmaceuticals, playing a crucial role in the development of new compounds and medications.
Used in Antioxidant Applications:
Due to its antioxidant properties, 1-(1,4-dihydroxynaphthalen-2-yl)ethanone is used to protect products from oxidative damage, extending their shelf life and maintaining their quality.
Used in Sunscreen Formulations:
Diosone has shown potential as a photostabilizer in sunscreen formulations, helping to stabilize the product and protect it from the degrading effects of sunlight.
Check Digit Verification of cas no
The CAS Registry Mumber 40420-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40420-48:
(7*4)+(6*0)+(5*4)+(4*2)+(3*0)+(2*4)+(1*8)=72
72 % 10 = 2
So 40420-48-2 is a valid CAS Registry Number.
40420-48-2Relevant academic research and scientific papers
Kise, Naoki,Yamamoto, Shota,Sakurai, Toshihiko
, p. 13973 - 13982 (2020)
Electroreductive coupling of phthalic anhydrides with α,β-unsaturated carbonyl compounds in the presence of TMSCl and subsequent treatment with 1 M HCl gave 1,4-dihydroxynaphthalenes and 2-methyl-2,3-dihydronaphthalene-1,4-diones.
An annulation reaction to naphthalene-1,4-diols using dimethyl phthalide-3-phosphonates
Watanabe,Morimoto,Nogami,Ijichi,Furukawa
, p. 968 - 970 (2007/10/02)
A regioselective annulation to naphthalene ring systems from dimethyl phthalide-3-phosphonates and electron-deficient olefins is described.