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4-Bromo-4'-hidroxibifenilo, 98 %, Thermo Scientific Chemicals

Catalog Number 11459762
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Cantidad:
5 g
25 g
100 g
Este artículo no se puede devolver. Vea la política de devoluciones
29558-77-8
C12H9BrO
249.107
MFCD00059076
ARUBXNBYMCVENE-UHFFFAOYSA-N
4-bromo-4'-hydroxybiphenyl, 4'-bromo-1,1'-biphenyl-4-ol, 4-4-bromophenyl phenol, 4'-bromobiphenyl-4-ol, 4-hydroxy-4'-bromobiphenyl, 1,1'-biphenyl-4-ol, 4'-bromo, 4-bromo-4-hydroxybiphenyl, pubchem23025
95093
4-(4-bromofenil)fenol
C1=CC(=CC=C1C2=CC=C(C=C2)Br)O
Este artículo no se puede devolver. Vea la política de devoluciones
29558-77-8
C12H9BrO
249.107
MFCD00059076
ARUBXNBYMCVENE-UHFFFAOYSA-N
4-bromo-4'-hydroxybiphenyl, 4'-bromo-1,1'-biphenyl-4-ol, 4-4-bromophenyl phenol, 4'-bromobiphenyl-4-ol, 4-hydroxy-4'-bromobiphenyl, 1,1'-biphenyl-4-ol, 4'-bromo, 4-bromo-4-hydroxybiphenyl, pubchem23025
95093
4-(4-bromofenil)fenol
C1=CC(=CC=C1C2=CC=C(C=C2)Br)O

A biphenyl starting material. 4-Bromo-(1,1-biphenyl)-4-ol is a useful intermediate. Vinylation of 4-bromo-4-hydroxybiphenyl and ethyl acrylate using Pd (OAc) 2/PPh 3 catalyst was studied. Ethyl 4-(4-hydroxyphenyl) cinnamate was formed as the vinylation product, while, 4-hydroxybiphenyl and ethyl cinnamate were formed as side products. Preparation of 4-cyano-4'-hydroxybiphenyl This was prepared from 4-bromo-4'-benzenesulphonyloxybiphenyl by first hydrolysing it to 4-bromo-4-hydroxybiphenyl using sodium hydroxide dissolved in a mixture of water and dioxan. The syntheses of the Nanocomposite dendrimers based on cyclic phosphazene cores: Amorphous materials, were accomplished by following a modified literature procedure by reacting phosphonitrilic chloride trimer with 4-bromophenol or 4-bromo-4-hydroxybiphenyl, respectively, in the presence of K 2 CO 3 in tetrahydrofuran (THF).

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
Un material de partida de bifenilo. 4′El -bromo-(1,1′-bifenil)-4-ol es un intermedio útil. Se estudió la vinilación de 4-bromo-4′-hidroxibifenilo y acrilato de etilo utilizando el catalizador Pd (OAc) 2/PPh 3 El cinnamato de etilo 4-(4′-hidroxifenilo) se formó como producto de vinilación, mientras que el 4-hidroxibifenilo y el cinnamato de etilo se formaron como productos secundarios. Preparación de 4-ciano-4′-hidroxibifenilo se preparó a partir de 4-bromo-4′-bencenosulfoniloxibifenilo por primera hidrolizando a 4-bromo-4-hidroxibifenilo mediante hidróxido sódico disuelto en una mezcla de agua y dioxano. Las síntesis de los dendrímeros nanocompuestos basados en núcleos de fosfaceno cíclico: Los materiales amorfos, se realizaron siguiendo un procedimiento de literatura modificado, reaccionando el trímero de cloruro fosfonitrílico con 4-bromofenol o 4-bromo-4′-hidroxibifenilo, respectivamente, en presencia de K 2 CO 3 en tetrahidrofurano (THF).

Solubilidad
Soluble en agua (parcialmente) y metanol.

Notas
Almacenar en un lugar fresco. Mantener el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar alejado de agentes oxidantes fuertes.
TRUSTED_SUSTAINABILITY
Nombre del producto químico o material 4-Bromo-4'-hydroxybiphenyl
Punto de fusión 163°C to 168°C
Cantidad 100 g
Información de solubilidad Soluble in water (partly),and methanol.
Formula Weight (peso de la fórmula) 249.11
Porcentaje de pureza 98%

RUO – Research Use Only

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