84212-57-7 Usage
Description
1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is a chemical compound derived from curcumin, a natural compound found in turmeric. It possesses anti-inflammatory, antioxidant, and anti-cancer properties due to its phenolic and methoxy groups, which contribute to its potential therapeutic effects. 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is currently under research for its promising applications in various diseases and health conditions.
Uses
Used in Pharmaceutical Applications:
1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is used as a potential therapeutic agent for its anti-inflammatory, antioxidant, and anti-cancer properties. 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione's phenolic and methoxy groups contribute to its therapeutic effects, making it a promising candidate for the treatment of various diseases and health conditions.
Used in Antioxidant Applications:
In the field of antioxidants, 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is used for its antioxidant activity. The phenolic groups in the compound are known for their ability to neutralize free radicals, which can help protect cells from oxidative stress and damage.
Used in Anti-inflammatory Applications:
1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is used as an anti-inflammatory agent. Its anti-inflammatory properties can be beneficial in treating conditions characterized by inflammation, such as arthritis or other inflammatory diseases.
Used in Cancer Research:
In cancer research, 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione is used for its anti-cancer properties. 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione has shown potential in inhibiting cancer cell growth and proliferation, making it a promising candidate for further research and development in the field of oncology.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic outcomes of 1-(4,6-dimethoxy-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propan-1,3-dione, novel drug delivery systems are being developed. These systems aim to improve the compound's delivery to target cells, increasing its efficacy and potential applications in various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 84212-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,1 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84212-57:
(7*8)+(6*4)+(5*2)+(4*1)+(3*2)+(2*5)+(1*7)=117
117 % 10 = 7
So 84212-57-7 is a valid CAS Registry Number.
84212-57-7Relevant articles and documents
Preparation method and application of tricetin
-
Paragraph 0007; 0052; 0063; 0068; 0069, (2019/10/01)
The invention belongs to the field of medicine synthesis, and in particular relates to a preparation method and application of tricetin. The method comprises the following steps: performing hydroxy protection to form a compound 3 by using 2,4,6-trihydroxyacetophenone as a starting material, performing an acylation reaction on the compound 3 and 3,4,5-trimethoxybenzoyl chloride to form a compound 4, performing Baker-Venkataranan rearrangement on the compound 4 to form a compound 5, performing cyclization on the compound 5 under catalysis of H2SO4/HOAc to form a compound 6, and finally performing pyridine hydrochloride deprotection on the compound 6 to form the tricetin, wherein in the step of synthesizing the compound 5, when NaOH is selected as a base and pyridine is selected as a solvent,the yield is greatly improved, and the reaction is relatively stable. According to the method provided by the invention, pharmacological activity experiments show that the compound synthesized by themethod has anti-nerve damage activity, so that the compound has better application prospects in treating nerve damage-related diseases.
The Preparation of Flavones and their Derivatives. Part I. Flavones and 4-Thioflavones.
Briggs, Malcolm T.,Duncan, Graham L. S.,Thornber, Craig W.
, p. 2461 - 2487 (2007/10/02)
A series of polysubstituted flavones has been prepared with particular emphasis on 3',4',5',5,7-pentahydroxyflavone and its ether derivatives.The preparation of 4-thioflavones has been undertaken to provide intermediates for the preparation of 4-iminoflav
