2,4-Dibromophenol

Last updated
2,4-Dibromophenol
2,4-Dibromophenol.svg
Names
Preferred IUPAC name
2,4-Dibromophenol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.009.488 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 210-446-5
PubChem CID
UNII
  • InChI=1S/C6H4Br2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H
    Key: FAXWFCTVSHEODL-UHFFFAOYSA-N
  • c1cc(c(cc1Br)Br)O
Properties
C6H4Br2O
Molar mass 251.905 g·mol−1
Melting point 38 °C (100 °F; 311 K)
Boiling point 238.5 °C (461.3 °F; 511.6 K)
Hazards
GHS labelling:
GHS-pictogram-skull.svg GHS-pictogram-exclam.svg
Danger
H300, H315, H319, H335, H412
P261, P264, P270, P271, P273, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2,4-Dibromophenol is an isomer of dibromophenol with the molecular formula C6H4Br2O.

Contents

Properties

At room temperature, 2,4-dibromophenol is a solid with needle-like crystals. It melts at 38 °C (100.4 °F) and boils at 238.5 °C (461.3 °F). it has a molecular weight of 251.905 g/mol. It is soluble in water, ethanol, ether and benzene and slightly soluble in carbon tetrachloride. [1]

Occurrence

2,4-Dibromophenol is found in certain molluscs and crustaceans, [1] as well as the acorn worm Saccoglossus bromophenolosus , which is named after it. [2]

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3
COCHCOCH
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) and metal ions, usually transition metals. The bidentate ligand acetylacetonate is often abbreviated acac. Typically both oxygen atoms bind to the metal to form a six-membered chelate ring. The simplest complexes have the formula M(acac)3 and M(acac)2. Mixed-ligand complexes, e.g. VO(acac)2, are also numerous. Variations of acetylacetonate have also been developed with myriad substituents in place of methyl (RCOCHCOR). Many such complexes are soluble in organic solvents, in contrast to the related metal halides. Because of these properties, acac complexes are sometimes used as catalyst precursors and reagents. Applications include their use as NMR "shift reagents" and as catalysts for organic synthesis, and precursors to industrial hydroformylation catalysts. C
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H
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in some cases also binds to metals through the central carbon atom; this bonding mode is more common for the third-row transition metals such as platinum(II) and iridium(III).

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References

  1. 1 2 CID 12005 from PubChem
  2. Konikoff, Charlotte (2017). "Saccoglossus bromophenolosus King, Giray & Kornfield, 1994". WoRMS. World Register of Marine Species . Retrieved 31 August 2017.