2-Bromofenol, 98 %, Thermo Scientific Chemicals
2-Bromofenol, 98 %, Thermo Scientific Chemicals
2-Bromofenol, 98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Bromofenol, 98 %, Thermo Scientific Chemicals

CAS: 95-56-7 | C6H5BrO | 173.009 g/mol
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Cantidad:
25 g
100 g
500 g
Número de catálogo A14112.14
también denominado A14112-14
Precio (EUR)
99,65
Online exclusive
111,00
Ahorro 11,35 (10%)
Each
Cantidad:
25 g
Pedido a granel o personalizado
Precio (EUR)
99,65
Online exclusive
111,00
Ahorro 11,35 (10%)
Each
Identificadores químicos
CAS95-56-7
IUPAC Name2-bromophenol
Molecular FormulaC6H5BrO
InChI KeyVADKRMSMGWJZCF-UHFFFAOYSA-N
SMILESOC1=CC=CC=C1Br
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)Clear colorless to yellow or pale orange
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Refractive Index1.5870-1.5910 @ 20?C
FormLiquid
2-Bromophenol used as a disinfection byproduct found in chlorinated pool water. Used in the preparation of anti-benzofurobenzofuran diimides. It was also used to study the photodegradation of 2-bromophenol using UV-Vis spectroscopy and HPLC.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El 2-bromofenol se utiliza como derivado de desinfección en el agua de piscinas cloradas. Se utiliza en la preparación de diimidas de antibenzofurobenzofurano. También se ha utilizado para estudiar la fotodegradación del 2-bromofenol mediante espectroscopía UV-Vis y HPLC.

Solubilidad
Soluble en cloroformo y éter. Ligeramente soluble en agua.

Notas
Sensible a la luz. Almacenar en oscuridad. Almacenar en lugar fresco y seco, en recipientes herméticamente cerrados.
RUO – Research Use Only

General References:

  1. Sabin-Lucian Suraru et. al. Diindole-annulated naphthalene diimides: synthesis and optical and electronic properties of syn- and anti-isomers. Journal of Organic Chemistry. 2014, 79 (1), 128-139.
  2. Jayaraman A; Mas S; Tauler R, et al. Study of the photodegradation of 2-bromophenol under UV and sunlight by spectroscopic, chromatographic and chemometric techniques. J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 2012, 910 (1), 138-48.
  3. Reacts with n-BuLi to give a dilithio derivative, which reacts with electrophiles at carbon in a useful synthesis of ortho-substituted phenols: J. Org. Chem., 49, 5267 (1984).