597-01-3

Basic information

• Product Name: 1,4-bis(3,4-dimethoxyphenyl)dihydro-1H,3H-furo[3,4-c]furan-3a(4H)-ol
• Synonyms: 1H,3H-furo[3,4-c]furan-3a(4H)-ol, 1,4-bis(3,4-dimethoxyphenyl)dihydro-
• CAS NO: 597-01-3
• Molecular Formula: C₂₂H₂₆O₇
• Molecular Weight: 402.4376
• Mol File: 597-01-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 560.3°C at 760 mmHg
• Flash Point: 292.7°C
• Density: 1.253g/cm³
• Vapor Pressure: 2.17E-13mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: 1,4-bis(3,4-dimethoxyphenyl)dihydro-1H,3H-furo[3,4-c]furan-3a(4H)-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis(3,4-dimethoxyphenyl)dihydro-1H,3H-furo[3,4-c]furan-3a(4H)-ol(597-01-3)
• EPA Substance Registry System: 1,4-bis(3,4-dimethoxyphenyl)dihydro-1H,3H-furo[3,4-c]furan-3a(4H)-ol(597-01-3)

Safety Data

• Hazardous Substances Data: 597-01-3(Hazardous Substances Data)

Usage

Chemical structure

A complex organic compound with a furofuran backbone and two 3,4-dimethoxyphenyl groups.

Synonym

Bisfuranol.

Classification

Synthetic compound.

Application in organic synthesis

Used in organic synthesis and medicinal chemistry.

Biological activity

Has potential biological activity.

Potential therapeutic uses

Studied for its potential as an anti-inflammatory and anticancer agent.

Drug discovery and development

Its structure and properties make it a valuable tool for drug discovery and development.

Applications in materials science

May have applications in the field of materials science due to its unique structural features.
Please note that this list is based on the provided material and may not be exhaustive. Further research and analysis may reveal additional properties and applications of bisfuranol.

Upstream product

• 469-28-3 (+)-1-hydroxy-6-epipinoresinol 4',4''-di-O-methyl ether 
• 186581-53-3 diazomethane 
• 81426-18-8 (+)-1-hydroxypinoresinol 4''-O-methyl ether 
• 7553-56-2 iodine 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 56-23-5 tetrachloromethane 
• 81426-15-5 (+)-1-acetoxypinoresinol 4''-O-methyl ether 
• 96894-13-2 (+)-1-acetoxypinoresinol 
• 144918-25-2 (4S,5R)-4-(3,4-Dimethoxy-benzyloxymethyl)-5-(3,4-dimethoxy-phenyl)-dihydro-furan-3-one 
• 20583-78-2 ethyl (E)-3,4-dimethoxycinnamate 
• 144918-23-0 2-(3,4-dimethoxyphenyl)-3-(hydroxymethyl)-4-methylenetetrahydrofuran 
• 144918-22-9 ethyl rac-(2R,3R)-2-(3,4-dimethoxyphenyl)-4-methylenetetrahydrofuran-3-carboxylate 
• 144918-21-8 ethyl 2-bromo-3-(3,4-dimethoxyphenyl)-3-(prop-2-ynyloxy)propanoate 

Downstream Products

• 1212517-63-9 (3aS)-1c,4c-bis-(2-bromo-4,5-dimethoxy-phenyl)-(6ac)-dihydro-furo[3,4-c]furan-3ar-ol 
• 80900-39-6 2,5-bis(3,4-dimethoxyphenyl)-4-pyrone-3-aldehyde 
• 80900-41-0 2,5-bis(3,4-dimethoxyphenyl)-4-pyrone-3-carbinol 
• 252726-89-9 (1R,8S,9R,12S)-8-(3,4-Dimethoxy-phenyl)-12-hydroxymethyl-4,5-dimethoxy-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2,4,6-trien-12-ol 
• 124281-58-9 (2S,3R,4R)-4-(3,4-Dimethoxy-benzyl)-3-hydroxymethyl-2-(3-methoxy-phenyl)-tetrahydro-furan-3-ol 
• 124281-57-8 (1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-2,3-bis-hydroxymethyl-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ol 
• 124281-61-4 [(4aR,10R,10aR)-10-(3,4-Dimethoxy-phenyl)-7,8-dimethoxy-2,2-dimethyl-4,4a,5,10-tetrahydro-naphtho[2,3-d][1,3]dioxin-10a-yl]-methanol 
• 124281-60-3 C₂₅H₃₂O₇ 
• 124281-62-5 C₂₇H₃₄O₈ 
• 124281-59-0 Acetic acid (1R,2R,3R)-3-acetoxymethyl-1-(3,4-dimethoxy-phenyl)-2-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl ester 

Relevant articles and documents

Stereoselective Total Synthesis of (+/-)-Paulownin and (+/-)-Isogmelinol through Radical Annulation Route

A highly stereocontrolled synthesis of furofuran lignans, (+/-)-Paulownin (1a) and (+/-)-Isogmelinol (1b) is described involving intramolecular radical cyclisation as a key step.

Lignans from bark of the Olea plants. I

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