5026-12-0

Basic information

• Product Name: 2'-Hydroxy-2,4,4-triMethylflavan
• Synonyms: 2'-Hydroxy-2,4,4-triMethylflavan;2-(2,4,4-trimethyl-3H-chromen-2-yl)phenol
• CAS NO: 5026-12-0
• Molecular Formula: C₁₈H₂₀O₂
• Molecular Weight: 268.3502
• Mol File: 5026-12-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Solubility: DCM, Ethyl Acetate
• CAS DataBase Reference: 2'-Hydroxy-2,4,4-triMethylflavan(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-Hydroxy-2,4,4-triMethylflavan(5026-12-0)
• EPA Substance Registry System: 2'-Hydroxy-2,4,4-triMethylflavan(5026-12-0)

Safety Data

• Hazardous Substances Data: 5026-12-0(Hazardous Substances Data)

Usage

Uses

2''-Hydroxy-2,4,4-trimethylflavan is an impurity formed in the synthesis of Bisphenol A (B519495, a monomer used for policarbonate and epoxy resins.

Upstream product

• 917-64-6 methyl magnesium iodide 
• 486-58-8 disalicylide 
• 71-43-2 benzene 
• 67-64-1 acetone 
• 108-95-2 phenol 
• 3045-32-7 2-(1-hydroxy-1-methylethyl)phenol 
• 123-54-6 acetylacetone 
• 698-91-9 2-phenoxypropene 
• 4286-23-1 4-isopropenylphenol 
• 10277-93-7 2-isopropenylphenol 

Downstream Products

• 80-05-7 BPA 

Relevant articles and documents

One-pot synthesis of 4 h -chromenes by tandem benzylation and cyclization in the presence of sodium bisulfate on silica gel

A simple and efficient method has been developed for the synthesis of 4H-chromenes from o-hydroxybenzylic alcohols and dicarbonyl compounds containing active methylene groups by using silica gel supported sodium bisulfate. Various dicarbonyl compounds suc

REACTION OF PHENOL WITH ACETONE IN THE PRESENCE OF ALUMINUM PHENOLATE

The condensation of phenol with acetone in the presence of aluminum phenolate leads to a mixture of isomeric bis(hydroxyphenyl)propanes and 2'- and 4'-hydroxy-2,4,4-trimethylflavans, in which 2-(2-hydroxyphenyl)-2-(4-hydroxyphenyl)propane usually predominates.