758695-39-5 Usage
Chemical structure
A complex organic compound with a coumarin derivative core structure, consisting of a benzopyran ring system with two hydroxyl groups at the 4 and 5 positions, and a methoxy group at the 8 position.
Molecular weight
256.28 g/mol
Stereochemistry
The compound has a chiral center at the 1, 3, and 4 positions, with the (1R,3S,4S) configuration.
Natural occurrence
Daphnetin is found in various plants, making it a natural compound.
Pharmacological properties
Daphnetin has been studied for its potential anti-inflammatory, antioxidant, and anticancer activities.
Health benefits
The compound has been investigated for its effects on promoting bone and skin health.
Therapeutic potential
Daphnetin has been researched for its potential in treating various diseases, such as diabetes and cardiovascular disorders.
Interest in medicinal chemistry
Due to its diverse pharmacological properties and potential therapeutic applications, Daphnetin is an interesting compound for further exploration in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 758695-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,8,6,9 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 758695-39:
(8*7)+(7*5)+(6*8)+(5*6)+(4*9)+(3*5)+(2*3)+(1*9)=235
235 % 10 = 5
So 758695-39-5 is a valid CAS Registry Number.
758695-39-5Relevant academic research and scientific papers
Short, convergent, stereoselective syntheses of enantiopure 2-benzopyran-5,8-quinones related to the aphid insect pigments, the protoaphins
Birkbeck, Anthony A.,Brkic, Zinka,Giles, Robin G.F.
, p. 6147 - 6150 (2007/10/03)
The enantiopure (1S,3S,4R)-, (1R,3S,4S)- and (1S,3S,4S)-3,4-dihydro-1,3- dimethyl-4-hydroxy-2-benzopyrans 16, 25 and 26 are prepared in two related reaction sequences, each in eight steps and good overall yield. The starting materials are 4-methoxyphenol
The asymmetric synthesis of 2-benzopyrans and their quinones through intramolecular diastereoselective ring-closure of titanium phenolates of phenolic aldehydes
Giles, Robin G. F.,Joli, Cynthia A.
, p. 3039 - 3048 (2007/10/03)
Treatment of the phenolic aldehyde (a′5,25)-2-(5′-hydroxy-2′-methoxy-a′-methylbenzyloxy) propanal 15 with titanium tetraisopropoxide followed by ultrasonication led to its completely diastereoselective cyclisation in high yield to afford (lS,3S′,4.R)-3,4-
