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2,5-DIBROMOPHENOL

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2,5-DIBROMOPHENOL manufacturers

  • 2,5-DIBROMOPHENOL
  • 2,5-DIBROMOPHENOL pictures
  • 2026-06-30
  • CAS:28165-52-8
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 10000KGS
  • 2,5-DIBROMOPHENOL
  • 2,5-DIBROMOPHENOL pictures
  • $6.60
  • 2019-12-31
  • CAS:28165-52-8
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 1kg-1000kg
2,5-DIBROMOPHENOL Basic information
Product Name:2,5-DIBROMOPHENOL
Synonyms:2,5-Dibromophenol 98%;2,5-Dibromophenol 96+%;2,5-Dibromo-1-hydroxybenzene;Phenol, 2,5-dibromo-;2,5-Dibromophenol@100 μg/mL in Toluene;2,5-Dibromophenol in isopropanol
CAS:28165-52-8
MF:C6H4Br2O
MW:251.9
EINECS:
Product Categories:
Mol File:28165-52-8.mol
2,5-DIBROMOPHENOL Structure
2,5-DIBROMOPHENOL Chemical Properties
Melting point 73-74 °C
Boiling point 244.6±20.0 °C(Predicted)
density 2.095±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form powder
pka7.47±0.10(Predicted)
color White
InChIInChI=1S/C6H4Br2O/c7-4-1-2-5(8)6(9)3-4/h1-3,9H
InChIKeyGUXWVUVLXIJHQF-UHFFFAOYSA-N
SMILESC1(O)=CC(Br)=CC=C1Br
Safety Information
HS Code 2908190090
MSDS Information
2,5-DIBROMOPHENOL Usage And Synthesis
Chemical Properties2,5-Dibromophenol is a white to pale yellow powder, slightly soluble in water, very slightly soluble in chloroform and methanol. It should be stored under an inert atmosphere and at room temperature to maintain its stability.
Uses2,5-Dibromophenol is an important intermediate in organic synthesis and is often used to synthesize other complex organic molecules.
Synthesis
2,5-Dibromobenzenamine

3638-73-1

2,5-DIBROMOPHENOL

28165-52-8

General procedure for the synthesis of 2,5-dibromophenol from 2,5-dibromoaniline: Sodium nitrite (65.2 mmol) was added in batches to a solution of trifluoroacetic acid (80 mL) containing 2,5-dibromoaniline (55.8 mmol) at 0 °C. Subsequently, the resulting solution was slowly added to a boiling solution of 50% sulfuric acid (120 mL) containing sodium sulfate (10 g) and the reaction mixture was kept at reflux for 1 hour. Upon completion of the reaction, the product was steam distilled and the distillate was extracted using dichloromethane (2 x 200 mL). The organic layers were combined, dried over sodium sulfate and concentrated to give 2,5-dibromophenol as a yellow solid in 41% yield.

References[1] Environmental Science and Technology, 2001, vol. 35, # 18, p. 3749 - 3756
[2] Patent: WO2009/23844, 2009, A2. Location in patent: Page/Page column 129-130
[3] Patent: US2010/16297, 2010, A1. Location in patent: Page/Page column 33-34
[4] Patent: WO2010/21797, 2010, A1. Location in patent: Page/Page column 94-95
[5] Patent: US2010/29629, 2010, A1. Location in patent: Page/Page column 62
2,5-DIBROMOPHENOL Preparation Products And Raw materials
Raw materials2,5-Dibromobenzenamine
Preparation Products2,5-DIBROMOANISOLE
Tag:2,5-DIBROMOPHENOL(28165-52-8) Related Product Information
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