20321-73-7 Usage
Uses
Used in Pharmaceutical Industry:
2,2-DIMETHYL-7-METHOXY-4-CHROMANONE is used as an antioxidant and anti-inflammatory agent for its potential therapeutic benefits in treating various conditions. Its antioxidant properties help protect cells from damage caused by free radicals, while its anti-inflammatory effects can alleviate inflammation-related disorders.
Used in Cosmetic Industry:
In the cosmetic industry, 2,2-DIMETHYL-7-METHOXY-4-CHROMANONE is used as an active ingredient for its antioxidant and anti-inflammatory properties. It can help protect the skin from environmental stressors and reduce inflammation, leading to improved skin health and appearance.
Used in Food and Beverage Industry:
2,2-DIMETHYL-7-METHOXY-4-CHROMANONE is used as a flavoring agent in food and beverages. Its unique taste and aroma can enhance the sensory experience of various products, making them more appealing to consumers.
Used in Neuroprotective Research:
2,2-DIMETHYL-7-METHOXY-4-CHROMANONE has been studied for its potential neuroprotective effects. It may have the ability to protect neurons from damage and degeneration, which could be beneficial in the development of treatments for neurodegenerative diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 20321-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20321-73:
(7*2)+(6*0)+(5*3)+(4*2)+(3*1)+(2*7)+(1*3)=57
57 % 10 = 7
So 20321-73-7 is a valid CAS Registry Number.
20321-73-7Relevant articles and documents
β,β-dimethylacrylophenones : BF3.ET2O-POCl3 catalysed acylation of phenols using β, β-dimethylacrylic acid
Jain, Niveta,Krishnamurty
, p. 1237 - 1241 (2007/10/03)
Boron trifluoride etherate - phosphoryl chloride reagent is a useful reagent for the condensation between phenols and β,β-dimethylacrylic acid. The main products are acrylophenones. But surprisingly hydroquinone gives mono and diacrylates.
ON THE REACTION OF SUBSTITUTED PHENOLS AND 3-METHYLBUT-2-ENOIC ACID. A COMPARATIVE STUDY
Seboek, Peter,Jekoe, Jozsef,Timar, Tibor,Jaszberenyi, Joseph Cs.
, p. 2099 - 2114 (2007/10/02)
A systematic and comparative study of the reaction of a series of substituted phenols and 3-methylbut-2-enoic acid in zinc chloride/phosphorus oxychloride and aluminum chloride/phosphorus oxychloride reveals that the formation of phenolic esters and 2,2-dimethyl-4-chromanones is strongly influenced by the substituents, their popsition on the aromatic ring of the starting phenols.Based on our study, a mixed Friedel-Crafts and Fries rearrangement mechanism is in operation in these reactions.
On the synthesis of substituted 2,2-dimethyl1-4-chromanones and related compounds
Seboek, Peter,Jekoe, Jozsef,Timar, Tibor,Jaszberenyi, Joseph Cs.
, p. 2791 - 2794 (2007/10/02)
A systematic study of the reaction of a series of monosubstituted phenols 3 and 3-methylbut-2-enoic acid 4 in phosphorus oxychloride/zinc chloride revealed that the formation of 4-chromanones was strongly infuenced by the substituents and their position on the aromatic ring of the starting phenols.
