88256-04-6 Usage
Chemical class
Furan derivative
Structural features
Contains a furan ring
Three methoxy substituents on the furan ring
A hydroxyl group attached to the furan ring
Presence in nature
Identified in various plant species
Pharmacological properties
Antioxidant effects
Anti-inflammatory effects
Potential applications
Natural product for drug development
Antimicrobial activity against certain bacteria and fungi
Interest in fields of medicine and agriculture
This list provides a concise overview of the key characteristics and potential uses of 1,2,4-trimethoxydibenzo[b,d]furan-3-ol based on the information provided.
Check Digit Verification of cas no
The CAS Registry Mumber 88256-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88256-04:
(7*8)+(6*8)+(5*2)+(4*5)+(3*6)+(2*0)+(1*4)=156
156 % 10 = 6
So 88256-04-6 is a valid CAS Registry Number.
88256-04-6Relevant articles and documents
Boron Trichloride as a Selective Demethylating Agent for Hindered Ethers: a Synthesis of the Phytoalexins α- and β-Pyrufuran, a Synthesis of Tri-O-methylleprolomin and its Demethylation
Carvalho, Christopher F.,Russo, Albert V.,Sargent, Melvyn V.
, p. 777 - 792 (2007/10/02)
Boron trichloride has been found to be an efficient reagent for the selective cleavage of sterically hindered methoxy groups in methoxyarenes.The scope and utility of this reaction are explored with examples drawn from derivatives of benzene, naphtalene, 9,10-dihydrophenanthrene and dibenzofuran.The method is applied to the synthesis of the phytoalexins α- (56) and β-pyrofuran (58) (1,3,4-trimethoxydibenzofuran-2-ol and 1,2,4-trimethoxydibenzofuran-3-ol).A synthesis of tri-O-methylleprolomin (61), a derivative of the unusual lichen metabolite leprolomin (60), is described and its demethylation with boron trichloride is studied.
