94805-83-1 Usage
Uses
Used in Pharmaceutical Industry:
Isolicoflavonol is used as a bioactive compound for its potential antioxidant, anti-inflammatory, and anti-cancer properties. Its presence in various plants makes it a valuable resource for developing pharmaceutical products that can target a range of health issues.
Used in Nutraceutical Industry:
Isolicoflavonol is used as a dietary supplement for its potential health benefits, including improving cardiovascular health and reducing the risk of chronic diseases. Its antioxidant properties can help protect the body from oxidative stress and support overall well-being.
Used in Cosmetic Industry:
Isolicoflavonol is used as an ingredient in cosmetic products for its potential anti-aging and skin health benefits. Its antioxidant and anti-inflammatory properties can help protect the skin from environmental damage and promote a youthful appearance.
Used in Functional Food Industry:
Isolicoflavonol is used as an additive in functional foods for its potential health-promoting properties. Its presence in these foods can provide consumers with additional health benefits, such as improved cardiovascular health and reduced risk of chronic diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 94805-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94805-83:
(7*9)+(6*4)+(5*8)+(4*0)+(3*5)+(2*8)+(1*3)=161
161 % 10 = 1
So 94805-83-1 is a valid CAS Registry Number.
94805-83-1Relevant academic research and scientific papers
Synthesis method of isolicoflavonol
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, (2020/12/29)
The invention provides a synthesis method of isolicoflavonol, which comprises the following steps: carrying out condensation reaction on 2,4-O-R1(protective group, the same below)-6-hydroxyacetophenone and 4-O-R2(protective group, the same below)-benzaldehyde to generate 2',4'-O-R1-6'-hydroxy-4-O-R2-chalcone; oxidizing the chalcone to generate flavonol; carrying out selective protection on 3-OH ofthe flavonol to obtain 3,5,7-O-R1-4'-O-R2-flavonol; removing the protecting group R2 from the 3,5,7-O-R1-4'-O-R2-flavonol to obtain 3,5,7-O-R1-4'-hydroxyflavonol; carrying out 1,1-dimethylpropargyl reaction on the 4,4'-OH site to obtain 3,5,7-O-R1-4'-O-(1',1''-dimethyl propargyl)flavonol; carrying out partial hydrogenation on the alkynyl of the 3,5,7-O-R1-4'-O-(1',1''-dimethyl propargyl)flavonolunder the action of a catalyst to obtain 3,5,7-O-R1-4'-O-(1',1''-dimethylpropenyl)flavonol and carrying out Claisen rearrangement on the 3,5,7-O-R1-4'-O-(1',1''-dimethylpropenyl)flavonol to obtain 3,5,7-O-R1-isolicoflavonol, and removing the protecting group R1 from the 3,5,7-O-R1-isolicoflavonol to obtain the isolicoflavonol.
