4′-Hydroxy-3′-iodoacetophenone

• Catalog No.: 722057
• CAS Number: 62615-24-1
• M. F.: C8H7IO2
• M. W.: 262.04445
• Purity: 97%

SYNONYMS

• Title: 4′-羟基-3′-碘苯乙酮
• IUPAC name: 1-(4-hydroxy-3-iodophenyl)ethan-1-one
• IUPAC Traditional name: 1-(4-hydroxy-3-iodophenyl)ethanone
• Synonyms: 3-Iodo-4-hydroxyacetophenone; 2-Iodo-4-acetylphenol; 1-(4-羟基-3-碘苯基)乙酮; 4-Acetyl-2-iodophenol; 1-(4-Hydroxy-3-iodophenyl)ethanone

DATABASE IDS

• MDL Number: MFCD06200221
• CAS Number: 62615-24-1

PROPERTIES

• Empirical Formula (Hill Notation): C8H7IO2
• Purity: 97%
• Melting Point: 155-160 °C
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H318
• European Hazard Symbols: Harmful (Xn)
• GHS Precautionary statements: P280-P305 + P351 + P338
• Risk Statements: 22-41
• Safety Statements: 26-39
• German water hazard class: 1

DETAILS

Description (简体中文)

包装
5 g in glass bottle
Application
Reactant for:
• Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes1
• Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction2
• Regioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in air3
• Preparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclization4
• Stereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenes5
• Preparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynes6
• Preparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina7

Description (English)

Packaging
5 g in glass bottle
Application
Reactant for:
• Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes1
• Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction2
• Regioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in air3
• Preparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclization4
• Stereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenes5
• Preparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynes6
• Preparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina7