121587-20-0 Usage
Description
(2R,3R)-2-(4-Hydroxy-3-methoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-1,4,5-trioxa-phenanthren-6-one, also known as tricin, is a naturally occurring flavonoid found in various plants. It is known for its antioxidant, anti-inflammatory, and anti-cancer properties. Tricin has been studied for its potential to inhibit the growth of cancer cells and to reduce inflammation in the body. It is also being researched for its potential therapeutic applications in the treatment of various diseases and conditions. Additionally, tricin has been found to have neuroprotective effects and may play a role in supporting overall brain health.
Uses
Used in Pharmaceutical Industry:
Tricin is used as a therapeutic agent for its potential anti-cancer properties, as it has been studied for its ability to inhibit the growth of cancer cells.
Used in Nutraceutical Industry:
Tricin is used as a dietary supplement for its antioxidant and anti-inflammatory properties, which may help reduce inflammation in the body and support overall health.
Used in Neuroprotective Applications:
Tricin is used as a neuroprotective agent for its potential to support brain health and protect against neurodegenerative diseases.
Used in Cosmetic Industry:
Tricin is used as an ingredient in cosmetic products for its antioxidant properties, which may help protect the skin from damage and promote a youthful appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 121587-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121587-20:
(8*1)+(7*2)+(6*1)+(5*5)+(4*8)+(3*7)+(2*2)+(1*0)=110
110 % 10 = 0
So 121587-20-0 is a valid CAS Registry Number.
121587-20-0Relevant articles and documents
Synthesis and Structural Elucidation of Coumarinolignans
Lin, Lee-Juian,Cordell, Geoffrey A.
, p. 3052 - 3080 (2007/10/02)
Coumarinolignans are a relatively new class of natural products combining a coumarin skeleton with a phenylpropene moiety.We describe here details of the first biomimetic syntheses of compounds in this series (1-16) utilizing both chemical and enzymatic approaches and the application of the selective INEPT nmr technique for unambiguous structure assignment.Chemical oxidation using silver oxide as an oxidizing agent typically produced two regioisomeric trans-substituted coumarinolignans.Enzymatic oxidation on the other hand normally gave rise to a single regioisomer.Almost all of the known natural coumarinolignans and several new compounds which may subsequently be obtained as natural products were synthesized.Three nmr strategies are described for the structure elucidation of the coumarinolignans, but only one of these techniques, the selective INEPT method, affords an unambiguous structure when only one regioisomer is present.Using this technique the structures and complete proton and carbon-13 chemical shift assignments of sixteen synthetic coumarinolignans were established.The described nmr strategy should prove useful for the unambiguous structure determination of all natural 2-aryl benzodioxanes, including the flavonolignans, the xanthonolignans and certain neolignans.
