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

2,2'-Dihydroxybiphenyl, 99%

CAS: 1806-29-7 | C12H10O2 | 186.21 g/mol
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Catalog number A14800.22
also known as A14800-22
Price (EUR)
48,90
Each
Quantity:
100 g
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Price (EUR)
48,90
Each
Chemical Identifiers
CAS1806-29-7
IUPAC Name[1,1'-biphenyl]-2,2'-diol
Molecular FormulaC12H10O2
InChI KeyIMHDGJOMLMDPJN-UHFFFAOYSA-N
SMILESOC1=CC=CC=C1C1=CC=CC=C1O
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SpecificationsSpecification SheetSpecification Sheet
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.

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

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. 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.
  2. 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.
  3. 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).