93727-83-4

Basic information

• Product Name: 4,4'-(5-hydroxypentane-2,2-diyl)diphenol
• Synonyms: 4,4'-(5-hydroxypentane-2,2-diyl)diphenol
• CAS NO: 93727-83-4
• Molecular Weight: 272.344
• Mol File: 93727-83-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,4'-(5-hydroxypentane-2,2-diyl)diphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-(5-hydroxypentane-2,2-diyl)diphenol(93727-83-4)
• EPA Substance Registry System: 4,4'-(5-hydroxypentane-2,2-diyl)diphenol(93727-83-4)

Safety Data

• Hazardous Substances Data: 93727-83-4(Hazardous Substances Data)

Upstream product

• 126-00-1 4,4-bis(4-hydroxyphenyl)valeric acid 
• 7297-85-0 4-hydroxy-γ-(4-hydroxyphenyl)-γ-methyl-benzenebutanoic acid methyl ester 

Downstream Products

• 133472-85-2 -OH 
• 133472-87-4 -OH 
• 850233-94-2 4,4'-(5-bromopentane-2,2-diyl)diphenol 
• 1062142-22-6 C₄₁H₄₈O₇ 
• 1228438-33-2 C₉₉H₁₁₂O₁₅ 
• 1446029-48-6 4-(2-(4-(allyloxy)phenyl)5-hydroxypentan-2-yl)phenol 
• 1446029-50-0 4-(4-(allyloxy)phenyl)-4-(4-(4-formylphenoxy)phenyl)pentyl 2-bromo-2-methylpropanoate 
• 1446029-49-7 4-(4-(2-(4-(allyloxy)phenyl)5-hydroxypentan-2-yl)phenoxy)benzaldehyde 
• 1397706-67-0 4,4'-bis(4-(4-formylphenoxy)phenyl)pentyl 2-bromopropanoate 
• 1397706-66-9 4,4'-(4,4'-(5-hydroxypentane-2,2-diyl)bis(4,1-phenylene))bis(oxy)dibenzaldehyde 

Relevant articles and documents

2, 2'-BIS (4-HYDROXYPHENYL) ALKYL AZIDES AND PROCESS FOR THE PREPARATION THEREOF

The application discloses monomers based on bis phenols with pendent reactive azido groups. The application further provides a process for preparation of bisphenol monomers with pendent reactive azido groups which are used further for preparing polymers w

Aromatic aldehyde functionalized polycaprolactone and polystyrene macromonomers: Synthesis, characterization and aldehyde-aminooxy click reaction

New bis-aldehyde functionalized initiators, viz, 4,4′-(4,4′-(5- hydroxypentane-2,2-diyl)bis(4,1-phenylene))bis(oxy)dibenzaldehyde (1) and 4,4′-bis(4-(4-(formylphenoxy) phenyl) pentyl 2-bromopropanoate (2) were synthesized starting from commercially available 4,4′-bis(4-hydroxyphenyl) pentanoic acid. These initiators were utilized, respectively, for ring opening polymerization of -caprolactone and atom transfer radical polymerization of styrene. Well-defined polycaprolactone macromonomers (MnGPC: 2600-19400, PDI: 1.37-1.47) and polystyrene macromonomers (MnGPC: 2800-28200, PDI: 1.11-1.16) with bis-aldehyde functionality were synthesized. The kinetic study of styrene polymerization showed controlled polymerization behaviour. The presence of aldehyde functionality in macromonomers was confirmed by 1H NMR spectroscopy. The reactivity of aldehyde functionality was demonstrated by carrying out aldehyde-aminooxy click reaction of polycaprolactone macromonomer with O-(2-azidoethyl) hydroxylamine which proceeded in a quantitative manner without backbone degradation.

Hyperbranched Macromolecules via a Novel Double-Stage Convergent Growth Approach

A novel double-stage convergent growth approach for the preparation of dendritic macromolecules is described. In the first stage, convergent growth with 4,4-bis(4′-hydroxyphenyl)pentanol as the building block is used to create symmetrical dendritic struct