24258-36-4 Usage
Uses
Used in Pharmaceutical Applications:
Umbelliferone is utilized as a pharmaceutical agent for its potential therapeutic effects in treating various diseases and disorders. Its antioxidant, anti-inflammatory, and anti-tumor properties make it a promising candidate for further research and development in the medical field.
Used in Cosmetic and Fragrance Industry:
In the cosmetic and fragrance industry, umbelliferone is used as a fragrance ingredient due to its pleasant odor. Its natural origin and appealing scent make it a desirable component in various cosmetic products.
Used in Biological Research:
Umbelliferone is employed as a fluorescent dye in biological research. Its fluorescent properties allow for its use in various applications, such as staining and visualization of biological samples, making it a valuable tool for researchers in the life sciences.
Used in Antioxidant Applications:
Umbelliferone is used as an antioxidant agent, helping to protect cells from oxidative damage and potentially reducing the risk of various diseases associated with oxidative stress.
Used in Anti-inflammatory Applications:
Due to its anti-inflammatory properties, umbelliferone is used in applications targeting the reduction of inflammation, which can be beneficial in treating conditions characterized by excessive inflammation.
Used in Anti-tumor Applications:
Umbelliferone is used as an anti-tumor agent, showing potential in inhibiting tumor growth and progression, making it a candidate for further exploration in oncology research.
Check Digit Verification of cas no
The CAS Registry Mumber 24258-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24258-36:
(7*2)+(6*4)+(5*2)+(4*5)+(3*8)+(2*3)+(1*6)=104
104 % 10 = 4
So 24258-36-4 is a valid CAS Registry Number.
24258-36-4Relevant academic research and scientific papers
High-selectivity preparation method for 7-methoxy-6/8-hydroxy coumarin
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Paragraph 0048; 0049; 0050, (2017/08/28)
The invention provides a high-selectivity preparation method for 7-methoxy-6/8-hydroxy coumarin and belongs to the field of synthesis of natural medicines. The method comprises the steps of subjecting a catechol coumarin compound to a high-selectivity methylation reaction with a methylation reagent in a proper base catalyst added organic reaction system, so as to obtain a 7-hydroxyl mono-methylate, wherein the mole ratio of a base to the catechol coumarin compound is (2.0 to 7.0): 1, the mole ratio of the methylation reagent to the catechol coumarin compound is (1.0 to 3.0): 1, the temperature of the organic reaction system is 0 DEG C to 30 DEG C, and the reaction time is 1.0 to 5.0 hours. The method has the characteristics of simplicity in operation, moderate conditions, good selectivity, high yield and the like and can be applied to the preparation of mono-methylates of coumarin catechols with different types of substituents.
Neoflavonoids as inhibitors of HIV-1 replication by targeting the Tat and NF-κB pathways
Olmedo, Dionisio A.,López-Pérez, José Luis,Del Olmo, Esther,Bedoya, Luis M.,Sancho, Rocío,Alcamí, José,Mu?oz, Eduardo,San Feliciano, Arturo,Gupta, Mahabir P.
, (2017/03/08)
Twenty-eight neoflavonoids have been prepared and evaluated in vitro against HIV-1. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase reporter gene. Inhibition of HIV transcription and Tat function were teste
