2,2'-Dihidroxibifenilo, 99 %, Thermo Scientific Chemicals

Name: 2,2'-Dihidroxibifenilo, 99 %, Thermo Scientific Chemicals
SKU: A14800.22

CAS: 1806-29-7 | C12H10O2 | 186.21 g/mol

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Cantidad:

25 g

100 g

500 g

Número de catálogo A14800.22

también denominado A14800-22

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Cantidad:

100 g

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Identificadores químicos

CAS1806-29-7

IUPAC Name[1,1'-biphenyl]-2,2'-diol

Molecular FormulaC12H10O2

InChI KeyIMHDGJOMLMDPJN-UHFFFAOYSA-N

SMILESOC1=CC=CC=C1C1=CC=CC=C1O

Especificaciones Specification Sheet

Hoja de especificaciones

Appearance (Color)Pale cream to pale brown

Assay (GC)≥98.5%

Melting Point (clear melt)106.0-113.0?C

FormPowder

2,2'-Dihydroxybiphenyl, is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.

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 2,2′-dihidroxibifenilo es una importante materia prima y un intermediario que se utiliza en síntesis orgánica, productos farmacéuticos, productos agroquímicos y colorantes.

Solubilidad
Insoluble en agua.

Notas
Almacenar en lugar fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Estable en las condiciones de almacenamiento recomendadas. Mantener alejado de agentes oxidantes fuertes.

RUO – Research Use Only

General References:

HP Kohler.; D Kohler-Staub. Degradation of 2-hydroxybiphenyl and 2, 2'-dihydroxybiphenyl by Pseudomonas sp. strain HBP1. Appl. Environ. Microbiol. 198854 (11), 2683-2688.
EJ Sohn.; CS Kim.; YS Kim.; DH Jung.; DS Jang.; YM Lee. Effects of magnolol (5, 5'-diallyl-2, 2'-dihydroxybiphenyl) on diabetic nephropathy in type 2diabetic Goto-Kakizaki rats. Life sciences. 200780 (5), 2683-2688.
Reacts with borane-THF to form the hydroborating agent 2,2'-biphenoxyborane (1,3,2-biphenyldioxaborepin). With this reagent cis-hydroboration is achieved with similar regioselectivity to catecholborane but greater reactivity: Heterocycles, 32, 425 (1991).