29558-78-9

Basic information

• Product Name: 4-HYDROXY-4'-IODOBIPHENYL
• Synonyms: 4-HYDROXY-4'-IODOBIPHENYL;4-(4'-IODOPHENYL)PHENOL;4-(4-IODOPHENYL)PHENOL;4-IODOBIPHENOL;4-Hydroxy-4'-iodobiphenyl;4'-Iodo-[1,1'-biphenyl]-4-ol
• CAS NO: 29558-78-9
• Molecular Formula: C₁₂H₉IO
• Molecular Weight: 296.1
• Product Categories: Aromatic Phenols;Biphenyl derivatives;Biphenyl & Diphenyl ether
• Mol File: 29558-78-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 117-119°C
• Boiling Point: 367.1 °C at 760 mmHg
• Flash Point: 175.8 °C
• Appearance: /
• Density: 1.689 g/cm³
• Storage Temp.: 2-8°C
• PKA: 9.65±0.26(Predicted)
• CAS DataBase Reference: 4-HYDROXY-4'-IODOBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-HYDROXY-4'-IODOBIPHENYL(29558-78-9)
• EPA Substance Registry System: 4-HYDROXY-4'-IODOBIPHENYL(29558-78-9)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21-36/37/38-65
• Safety Statements: 26-36/37/39-37
• Hazardous Substances Data: 29558-78-9(Hazardous Substances Data)

Usage

Uses

4-Hydroxy-4’-iodobiphenyl is a useful antifouling agent.

Upstream product

• 1204-79-1 4-amino-4'-hydroxybiphenyl 
• 7285-77-0 4-iodo-4'-aminobiphenyl 
• 179902-23-9 acetic acid-(4'-iodo-biphenyl-4-yl ester) 
• 134863-69-7 benzoic acid-(4'-iodo-biphenyl-4-yl ester) 
• 148-86-7 4-acetoxybiphenyl 
• 126971-87-7 4-iodo-4’-methoxy-1,1’-biphenyl 
• 10540-37-1 4-fluoro-4'-iodo-1,1'-biphenyl 
• 1591-31-7 4-iodo-biphenyl 

Downstream Products

• 134863-69-7 benzoic acid-(4'-iodo-biphenyl-4-yl ester) 
• 1034147-10-8 5-{[4-(4'-iodophenyl)phenyl]ethynyl}-2'-deoxyuridine 
• 51501-79-2 1,4'''-dimethoxy-4,1':4',1'':4'',1'''-quaterphenylene 
• 10508-41-5 4,4'''-dihydroxy-1,1':4',1'':4'',1'''-quaterphenyl 
• 126842-12-4 4,4'''-diacetoxy-p-quaterphenyl 
• 1221259-68-2 3-(1-adamantyl)-4'-iodobiphenyl-4-ol 
• 1030611-41-6 [4'-iodo-1,1'-biphenyl]-4-yl-1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylate 
• 1552276-80-8 1,4-bis[4-(4-bromophenyl)-1,4-bis(triethylsiloxy)-2,5-cyclohexadien-1-yl]benzene 

Relevant articles and documents

TEMPO-mediated late stage photochemical hydroxylation of biaryl sulfonium salts

The late stage photochemical hydroxylation of biaryl sulfonium salts was enabled with a TEMPO derivative as a simple oxygen source, in metal free conditions. The scope and mechanism of this exceptionally simple synthetic method, which constructs important arylated phenols from aromatic C-H bonds, are herein discussed.

Self-assembly of T-shaped aromatic amphiphiles into stimulus-responsive nanofibers

(Figure Presented) Stimulating fibers: Self-assembled nanofibers coated with hydrophilic oligo(ethylene oxide) dendrons transform reversibly, upon heating, into hydrophobic nanofiber bundles as a result of dehydration of the dendritic chains (see scheme). A thermoresponsive sol-gel phase transition is observed.