Fisetinidin chloride

Base Information

• Chemical Name: Fisetinidin chloride
• CAS No.: 2948-76-7
• Molecular Formula: C15H11 O5 . Cl
• Molecular Weight: 306.702
• UNII: MF2RUJ9T8H
• DSSTox Substance ID: DTXSID50583696
• Wikidata: Q5454453
• Wikipedia: Fisetinidin
• Mol file: 2948-76-7.mol

Synonyms:2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-1-benzopyrylium;2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-1-benzopyran-4-one;3,3',4',7-Tetrahydroxy-flavone;3,3',4',7-Tetrahydroxyflavone;5-Desoxy-quercetin;fisetin;fisetinidin

Chemical Property of Fisetinidin chloride

Chemical Property:

• Melting Point: 320℃
• Storage Temp.: −20°C
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 306.0295011
• Heavy Atom Count: 21
• Complexity: 336

Purity/Quality:

99.0% ^*data from raw suppliers

Fisetinidin chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): UN NO.
• Hazard Codes: UN NO.

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC(=CC2=[O+]C(=C(C=C21)O)C3=CC(=C(C=C3)O)O)O.[Cl-]
• Uses: Fisetinidin chloride is an antibacterial agent.

Technology Process of Fisetinidin chloride

There total 7 articles about Fisetinidin chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol (69082-77-5) → cyanidin chloride (528-58-5) + fisetinidin chloride (2948-76-7)

Guidance literature:

With hydrogenchloride; In isopropyl alcohol; at 97 ℃;

DOI:10.1039/P19810001220

Reference yield:

(2S,3S,4S)-4-(2,4-Dihydroxy-phenyl)-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol (65052-93-9,94942-00-4,125136-15-4,125136-16-5,125136-17-6,125136-18-7) → cyanidin chloride (528-58-5) + fisetinidin chloride (2948-76-7)

Guidance literature:

With hydrogenchloride; In isopropyl alcohol; at 97 ℃;

DOI:10.1039/P19810001220

Reference yield:

(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol (69082-77-5) → fisetinidin chloride (2948-76-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 30 mg / 0.05M benzophenone / acetone / Irradiation

2: 3M HCl / propan-2-ol / 97 °C

With hydrogenchloride; benzophenone; In isopropyl alcohol; acetone;

DOI:10.1039/P19810001220

upstream raw materials:

2,3’,4’-triacetoxyacetophenone

2,4-Dihydroxybenzaldehyde

(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol

(2S,3S,4S)-4-(2,4-Dihydroxy-phenyl)-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol

Downstream raw materials:

(+/-)-3c,7-Diacetoxy-2r-(3,4-diacetoxy-phenyl)-chroman

(+/-)-2r-(3,4-dihydroxy-phenyl)-chroman-3c,7-diol