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4-Bromocatechol

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4-Bromocatechol manufacturers

  • 4-BROMOCATECHOL
  • 4-BROMOCATECHOL pictures
  • 2026-03-20
  • CAS:17345-77-6
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20 mt
4-Bromocatechol Basic information
Product Name:4-Bromocatechol
Synonyms:4-Bromo-1,2-benzenediol;4-BROMO-1,2-DIHYDROXYBENZENE;4-bromopyrocatechol;1,2-Benzenediol, 4-broMo-;4-Bromocatechol>;-Bromocatechol;RMA-436;4-broMobenzene-1,2-diol
CAS:17345-77-6
MF:C6H5BrO2
MW:189.01
EINECS:241-370-5
Product Categories:
Mol File:17345-77-6.mol
4-Bromocatechol Structure
4-Bromocatechol Chemical Properties
Melting point 87 °C
Boiling point 280.5±20.0 °C(Predicted)
density 1.844±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO
form Solid
pka8.84±0.10(Predicted)
color Brown
Stability:Light Sensitive
InChIInChI=1S/C6H5BrO2/c7-4-1-2-5(8)6(9)3-4/h1-3,8-9H
InChIKeyAQVKHRQMAUJBBP-UHFFFAOYSA-N
SMILESC1(O)=CC=C(Br)C=C1O
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39-24/25
HS Code 29081990
MSDS Information
4-Bromocatechol Usage And Synthesis
Chemical PropertiesGrey powder
UsesA type of human dopamine sulfotransferase, belonging to the catechol family of molecules.
DefinitionChEBI: 4-Bromocatechol is a member of catechols.
Synthesis
Catechol

120-80-9

4-BROMOCATECHOL

17345-77-6

GENERAL METHODS: Catechol (1 mmol) was dissolved in acetonitrile (5 mL) and a magnetic stirrer was added to form a magnetically stirred solution. Subsequently, OXBTEATB (0.233 g, 0.5 mmol) was added to the solution and the reaction was stirred at room temperature for the reaction time referred to in Table 1.The reaction progress was monitored by thin layer chromatography (TLC) with an eluent ratio of hexane/ethyl acetate (5:1). Upon completion of the reaction, OXBTEATB was removed by filtration, and the filtrate was transferred to a partition funnel and extracted sequentially with water (15 mL) and dichloromethane (20 mL). The organic layer was collected and dried with anhydrous Na2SO4 and subsequently concentrated in a rotary evaporator to remove solvent. The crude product was purified by silica gel column chromatography, the eluent being a solvent mixture of hexane and ethyl acetate. To regenerate the reagents, the resulting white solid was treated with liquid bromine. The structures of all products were confirmed by determination of melting points or 1H NMR spectra and comparison with data reported in the literature [29a-29e].

References[1] Synthetic Communications, 2007, vol. 37, # 2, p. 323 - 328
[2] Organic letters, 2002, vol. 4, # 22, p. 3975 - 3978
[3] Molecules, 2014, vol. 19, # 3, p. 3401 - 3416
[4] Patent: US4791139, 1988, A
[5] Letters in Organic Chemistry, 2018, vol. 15, # 8, p. 682 - 687
4-Bromocatechol Preparation Products And Raw materials
Raw materialsAcetic acid-->Catechol-->4-Bromo-2-methoxyphenol-->5-Bromo-2-methoxyphenol-->Acetonitrile
Tag:4-Bromocatechol(17345-77-6) Related Product Information
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