199786-58-8

Basic information

• Product Name: 5-BROMO-2-IODOBENZENEMETHANOL
• Synonyms: 5-BROMO-2-IODOBENZENEMETHANOL;5-BROMO-2-IODOBENZYL ALCOHOL
• CAS NO: 199786-58-8
• Molecular Formula: C₇H₆BrIO
• Molecular Weight: 312.94
• Mol File: 199786-58-8.mol
• Article Data: 29

Chemical Properties

• Melting Point: 114-155 °C
• Boiling Point: 346.3±27.0 °C(Predicted)
• Appearance: /
• Density: 2.211±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 13.93±0.10(Predicted)
• CAS DataBase Reference: 5-BROMO-2-IODOBENZENEMETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-2-IODOBENZENEMETHANOL(199786-58-8)
• EPA Substance Registry System: 5-BROMO-2-IODOBENZENEMETHANOL(199786-58-8)

Safety Data

• Hazardous Substances Data: 199786-58-8(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-iodobenzenemethanol is a chemical compound with the molecular formula C7H6BrIO. It is a white to off-white solid that is used in various chemical and pharmaceutical applications. The compound is a derivative of benzene and contains both bromine and iodine atoms. It is commonly used as a building block in the synthesis of other organic compounds and as a reagent in chemical reactions. 5-Bromo-2-iodobenzenemethanol has potential applications in the pharmaceutical industry for the development of new drugs and in the production of specialty chemicals. It is important to handle and store this compound carefully, as it is potentially hazardous and can cause skin and eye irritation.

Upstream product

• 21740-00-1 5-bromo-2-iodo-benzoic acid 
• 181765-86-6 5-bromo-2-iodo-benzoic acid methyl ester 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 88-67-5 2-Iodobenzoic acid 
• 495414-06-7 4-bromo-2-(bromomethyl)-1-iodobenzene 
• 116632-39-4 2-methyl-4-bromoiodobenzene 
• 118-92-3 anthranilic acid 
• 5794-88-7 5-Bromo-2-aminobenzoic acid 

Downstream Products

• 689291-89-2 5-bromo-2-iodobenzaldehyde 
• 885693-79-8 2,5-bis((trimethylsilyl)ethynyl)benzaldehyde 
• 1038395-11-7 5-bromo-2-((triisopropylsilyl)ethynyl)benzaldehyde 
• 1038395-08-2 1,4-bis(5-bromo-2-iodostyryl)benzene 
• 1038395-09-3 C₄₂H₅₀Si₄ 
• 1038395-10-6 C₃₀H₁₈ 
• 1038395-15-1 C₆₂H₄₂O₈ 
• 1263055-18-0 2,5-diethynylbenzaldehyde 
• 1263055-20-4 C₂₇H₁₈O₅ 
• 1263055-24-8 2-((triisopropylsilyl)ethynyl)-5-((trimethylsilyl)ethynyl)benzaldehyde 
• 1263055-26-0 5-ethynyl-2-((triisopropylsilyl)ethynyl)benzaldehyde 
• 1263055-28-2 methyl 2-((3-formyl-4-((triisopropylsilyl)ethynyl)phenyl)ethynyl)benzoate 
• 1263055-30-6 methyl 2-((4-ethynyl-3-formylphenyl)ethynyl)benzoate 
• 1263055-32-8 C₂₇H₂₁NO₃ 

Relevant articles and documents

A new solvatochromic linear π-conjugated dye based on phenylene-(poly)ethynylene as supersensitive low-level water detector in organic solvents

A novel class of phenylene-(poly)ethynylene-based dye Sensor 1 with remarkable properties of solvatochromism has been designed and synthesized. A long, coplanar and asymmetry electron-rich π-conjugated structure endows Sensor 1 with maximum solvatochromic

Pd(II)-Catalyzed Synthesis of Benzocyclobutenes by β-Methylene-Selective C(sp3)-H Arylation with a Transient Directing Group

Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)-H arylation of ketones. The reaction utilizes glycine as a transient directing group and a 2-pyridone ligand, which may govern the methylene selectivity by making intimate molecular associations with the substrate during concerted metalation-deprotonation. This reaction is shown to be highly selective for intramolecular methylene C(sp3)-H arylation, thus enabling sequential C(sp3)-H functionalization.

CuSO4-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes

In this work, CuSO4 is utilized as a practical redox catalyst for tandem dual annulation in the synthesis of indole-fused tetracyclic heteroacenes, which are important skeletons in both medicinal chemistry and materials chemistry. The preparation of such skeletons in a convenient and efficient manner is in high demand. This method realizes the modular synthesis of benzofuro-, benzothieno-, and indoloindoles from abundant feedstocks such as 2-halobenzyl halides and nitrile derivatives in up to 99% yields, providing a rapid access to diverse indole-fused heteroacenes with biological or optoelectronic properties.