207115-22-8

Basic information

• Product Name: 4-BROMO-2-IODOPHENOL
• Synonyms: 4-BROMO-2-IODOPHENOL;2-Iodo-4-bromophenol;4-Bromo-2-iodophenol 98%;4-Bromo-2-iodophenol98%
• CAS NO: 207115-22-8
• Molecular Formula: C₆H₄BrIO
• Molecular Weight: 298.90383
• Mol File: 207115-22-8.mol

Chemical Properties

• Melting Point: 90℃ (ethanol )
• Boiling Point: 243.0±25.0℃ (760 Torr)
• Flash Point: 100.8±23.2℃
• Appearance: /
• Density: 2.369±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 7.94±0.18(Predicted)
• CAS DataBase Reference: 4-BROMO-2-IODOPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2-IODOPHENOL(207115-22-8)
• EPA Substance Registry System: 4-BROMO-2-IODOPHENOL(207115-22-8)

Safety Data

• Hazardous Substances Data: 207115-22-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-2-iodophenol is used as a key intermediate in the synthesis of pharmaceutical compounds for [application reason]. Its high reactivity and unique structure enable the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Bromo-2-iodophenol is utilized as a building block for the production of agrochemicals, such as pesticides and herbicides, for [application reason]. Its incorporation into these compounds enhances their effectiveness in controlling pests and weeds, contributing to increased crop yields and protection.
Used in Research Laboratories:
4-Bromo-2-iodophenol serves as a versatile reagent in research laboratories for conducting various chemical and biological experiments. Its unique properties make it suitable for use in [application reason], such as studying reaction mechanisms, testing hypotheses, and developing new methodologies in chemical synthesis and analysis.
Used in Material Science:
In the field of material science, 4-Bromo-2-iodophenol is employed as a component in the development of new materials and compounds for a wide range of industrial applications. Its unique structure and properties contribute to the creation of innovative materials with enhanced properties, such as improved stability, reactivity, or selectivity, for use in various industries.

InChI:InChI=1S/C6H4BrIO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H

Upstream product

• 533-58-4 2-Iodophenol 
• 40925-68-6 2-amino-4-bromo-phenol 
• 108-95-2 phenol 
• 106-41-2 4-bromo-phenol 
• 15459-51-5 2,6-di-iodo-4-bromophenol 

Downstream Products

• 1374302-95-0 2-(4-bromo-2-iodophenoxy)acetyl chloride 
• 1373233-46-5 6-bromo-4-butyl-2H-benzo[b][1,4]oxazin-3(4H)-one 
• 1374303-04-4 C₈H₆BrIO₃ 
• 1431639-03-0 C₁₇H₂₇BrOSi₂ 
• 1318697-61-8 C₁₂H₁₈BrIOSi 
• 1393671-28-7 (-)-4-bromo-1-{[(1R)-1-methyl-3-(4-methylphenyl)prop-2-yn-1-yl]oxy}-2-[(2-{[(1R)-1-methyl-3-(4-methylphenyl)prop-2-yn-1-yl]oxy}phenyl)ethynyl]benzene 
• 1393671-27-6 (-)-4-bromo-1-{[(1R)-1-methylprop-2-yn-1-yl]oxy}-2-[(2-{[(1R)-1-methylprop-2-yn-1-yl]oxy}phenyl)ethynyl]benzene 
• 1393671-26-5 (-)-[(3R)-3-(2-{[5-bromo-2-({(1R)-1-methyl-3-[tris(1-methylethyl)silyl]prop-2-yn-1-yl}oxy)phenyl]ethynyl}phenoxy)but-1-yn-1-yl][tris(1-methylethyl)]silane 
• 1393671-25-4 C₁₉H₂₈BrIOSi 
• 1393671-24-3 (+)-4-bromo-2-iodo-1-{[(1R)-1-methylprop-2-yn-1-yl]oxy}benzene 
• 1374995-64-8 C₃₃H₃₂BrNO₇ 
• 1374995-62-6 C₃₃H₃₂BrNO₇ 
• 1374995-76-2 C₁₆H₁₈BrNO₄ 
• 13141-26-9 5-bromo-2-phenylbenzo[b]furan 

Relevant articles and documents

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Regioselective monobromination of phenols with KBr and ZnAl–BrO3?–layered double hydroxides

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