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Protostephanone is a natural chemical compound found in certain plant species, particularly in the genus of Stephania. It is a yellow crystalline solid with a slightly floral and fruity odor. Known for its potential medicinal properties, including anti-inflammatory and anti-cancer effects, it has garnered interest among researchers and scientists for its unique chemical structure and promising therapeutic applications.

20824-18-4

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20824-18-4 Usage

Uses

Used in Pharmaceutical Industry:
Protostephanone is used as a pharmaceutical agent for its anti-inflammatory and anti-cancer effects. Its potential medicinal properties make it a candidate for further drug development and scientific exploration, particularly in the treatment of various inflammatory and cancerous conditions.
Used in Cosmetic Industry:
In the cosmetic industry, Protostephanone is used as a fragrance and flavoring agent due to its slightly floral and fruity odor. Its natural origin and pleasant scent make it a desirable ingredient in various cosmetic products.
Used in Food Industry:
Similarly, in the food industry, Protostephanone is utilized as a flavoring agent, adding a unique and appealing taste to various food products. Its natural and safe profile makes it a preferred choice for enhancing the flavor of food items.

Check Digit Verification of cas no

The CAS Registry Mumber 20824-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,2 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20824-18:
(7*2)+(6*0)+(5*8)+(4*2)+(3*4)+(2*1)+(1*8)=84
84 % 10 = 4
So 20824-18-4 is a valid CAS Registry Number.

20824-18-4Downstream Products

20824-18-4Relevant academic research and scientific papers

Synthesis along Biosynthetic Pathways. Part 2. Synthesis of Protostephanine

Battersby, Alan R.,Bhatnagar, Akil K.,Hackett, Peter,Thornber, Craig W.,Staunton, James

, p. 2002 - 2009 (2007/10/02)

The dienone protostephanone (3) is synthesised by phenol coupling or by Pschorr cyclisation from readily prepared tetrahydroisoquinolines, and the corresponding dienols (17) and (18) are converted by rearrangement, fragmentation, and reduction into protostephanine (4).This sequence mimics the natural pathway to the alkaloid.

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