57526-59-7

Basic information

• Product Name: FISETINIDOL-(4B8)-CATECHIN
• Synonyms: FISETINIDOL-(4B8)-CATECHIN;fisetinidol-(4alpha,8)-catechin
• CAS NO: 57526-59-7
• Molecular Formula: C₃₀H₂₆O₁₁
• Molecular Weight: 562.52
• Mol File: 57526-59-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: FISETINIDOL-(4B8)-CATECHIN(CAS DataBase Reference)
• NIST Chemistry Reference: FISETINIDOL-(4B8)-CATECHIN(57526-59-7)
• EPA Substance Registry System: FISETINIDOL-(4B8)-CATECHIN(57526-59-7)

Safety Data

• Hazardous Substances Data: 57526-59-7(Hazardous Substances Data)

Usage

Description

Fisetinidol-(4B8)-Catechin is a unique ring assembly consisting of fisetinidol attached to a (+)-catechin unit, forming a bond between C-4 of the pyran ring and C-8 of the benzopyran ring. FISETINIDOL-(4B8)-CATECHIN is derived from Acacia mearnsii, a plant species known for its rich chemical composition and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
Fisetinidol-(4B8)-Catechin is used as a bioactive compound for its potential therapeutic properties. FISETINIDOL-(4B8)-CATECHIN's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs and therapies.
Used in Nutraceutical Industry:
Fisetinidol-(4B8)-Catechin is used as a key ingredient in the development of nutraceutical products due to its potential health benefits. Its presence in Acacia mearnsii suggests that it may contribute to the overall health-promoting properties of the plant, making it a valuable addition to dietary supplements and functional foods.
Used in Cosmetic Industry:
Fisetinidol-(4B8)-Catechin is used as an active ingredient in the cosmetic industry for its potential antioxidant and anti-aging properties. Its ability to interact with biological targets may help protect the skin from environmental stressors and promote a more youthful appearance.
Used in Agricultural Industry:
Fisetinidol-(4B8)-Catechin can be used as a natural pesticide or growth promoter in the agricultural industry. Its bioactive properties may help protect crops from pests and diseases while also promoting healthy growth and development.

Upstream product

• 967-27-1 (+)-mollisacacidin 
• 154-23-4 catechin 
• 104079-72-3 6-iodo-(+)-catechin 

Downstream Products

• 69082-83-3 (2R,3S,4S)-2,3-trans-3,4-trans-3-acetoxy-4-<(2R,3S)-2,3-trans-3-acetoxy-3',4',5,7-tetrametoxyflavan-8-yl>-3',4',7-trimethoxyflavan 
• 104079-73-4 (2R,3S,8R,9S,10R)-2,3-trans-8,9-trans-9,10-cis-3,9-diacetoxy-2,8-bis(3,4-dimethoxyphenyl)-10-(2,4-dimethoxyphenyl)-5-methoxy-3,4,9,10-tetrahydro-2H,8H-benzo<1,2-b; 3,4-b'>dipyran 
• 72258-70-9 (2R,3S,4R,2'R,3'S,2''R,3''S,4''S)-2,2',2''-Tris-(3,4-dihydroxy-phenyl)-3,4,3',4',3'',4''-hexahydro-2H,2'H,2''H-[4,6';8',4'']terchromene-3,7,3',5',7',3'',7''-heptaol 
• 72248-84-1 (2R,3S,4S,2'R,3'S,2''R,3''S,4''S)-2,2',2''-Tris-(3,4-dihydroxy-phenyl)-3,4,3',4',3'',4''-hexahydro-2H,2'H,2''H-[4,6';8',4'']terchromene-3,7,3',5',7',3'',7''-heptaol 
• 57499-11-3 (-)-fisetinidol-(4α,8)-(+)-catechin hepta-O-methyl 
• 102258-25-3 8,9-trans-9,10-cis-tetrahydropyrano<2,3-h>chromene 
• 118964-31-1 (2R,3S,4S,7S,8R)-2,8-Bis-(3,4-dihydroxy-phenyl)-4-(2,4-dihydroxy-phenyl)-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromene-3,5,7-triol 
• 119065-94-0 (2R,3S,4S,8R,9S)-2,8-Bis-(3,4-dihydroxy-phenyl)-4-(2,4-dihydroxy-phenyl)-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromene-3,5,9-triol 
• 105805-43-4 (2R,3S,4S,8S,9S)-2,8-Bis-(3,4-dihydroxy-phenyl)-4-(2,4-dihydroxy-phenyl)-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromene-3,5,9-triol 
• 119065-92-8 (2S,3S,8R,9S,10S)-2,8-Bis-(3,4-dihydroxy-phenyl)-10-(2,4-dihydroxy-phenyl)-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromene-3,5,9-triol 
• 104113-23-7 (2R,3S)-2,3-trans-6-<(2R,3S,4R)-2,3-trans-3,4-cis-3,3',4',7-tetrahydroxyflavan-4-yl>-3,3',4',5,7-pentahydroxyflavan 
• 69176-55-2 (2R,3S)-2,3-trans-6-<(2R,3S,4S)-2,3-trans-3,4-trans-3,3',4',7-tetrahydroxyflavan-4-yl>-3,3',4',5,7-pentahydroxyflavan 
• 154-23-4 catechin 
• 155486-92-3 (2S)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)-propan-2-ol 

Relevant articles and documents

Synthesis of Condensed Tannins. Part 14. Biflavanoid Profisetinidins as Synthons. The Acid-Induced 'Phlobaphene'Reaction

Free phenolic - and -2,3-trans-(-)-fisetinidol-(+)-catechin diastereoisomers of both 3,4-trans and 3,4-cis configuration, which serve as synthons for higher oligomers, are available in improved yields from direct condensation, and also via novel 6-iodo-(+)-catechin as an intermediate substrate.Acid-induced transformations of the predominant -all-trans isomer, illustrative of the well-known 'phlobaphene reaction' of condensed tannins, is shown to include ring-isomerization and fission of the inter-flavanoid bond, followed in the latter instance by the alternatives of anthocyanidin formation, positional rearrangement and self-condensation.