2-Bromo-9H-xanthen-9-one

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2-Bromo-9H-xanthen-9-one manufacturers

  • 2-bromoxanthen-9-one
  • 2-bromoxanthen-9-one pictures
  • $2700.00
  • 2024-07-11
  • CAS:56341-31-2
  • Min. Order: 1Kg
  • Purity: 98
  • Supply Ability: 500 Kg
2-Bromo-9H-xanthen-9-one Basic information
Product Name:2-Bromo-9H-xanthen-9-one
Synonyms:2-BroMoxanthone;2-bromo-9-xanthenone;2-bromoxanthen-9-one;SBB010036;9H-Xanthen-9-one, 2-bromo-;2-bromo-1H-xanthen-9-one;Tributyl Phosphate Impurity 6(Tributyl Phosphate EP Impurity F);2-Bromo-9H-xanthen-9-one
CAS:56341-31-2
MF:C13H7BrO2
MW:275.1
EINECS:
Product Categories:
Mol File:56341-31-2.mol
2-Bromo-9H-xanthen-9-one Structure
2-Bromo-9H-xanthen-9-one Chemical Properties
Melting point 150 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling point 403.2±34.0 °C(Predicted)
density 1.620±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
InChIInChI=1S/C13H7BrO2/c14-8-5-6-12-10(7-8)13(15)9-3-1-2-4-11(9)16-12/h1-7H
InChIKeyDYQUGFRRGGOYCA-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=CC=C2)OC2=C1C=C(Br)C=C2
Safety Information
MSDS Information
2-Bromo-9H-xanthen-9-one Usage And Synthesis
Uses2-Bromoxanthone is part of a group of Xanthone (X500100) derivatives that belong to an important class of oxygenated heterocycles that have potential antitumour, antidiabetic and antihypertensive activity.
Synthesis
Benzaldehyde, 2-(4-bromophenoxy)-

364323-77-3

2-BROMO-9H-XANTHEN-9-ONE

56341-31-2

General procedure for the synthesis of 2-bromo-9H-xanthen-9-one from 2-(4-bromophenoxy)benzaldehyde: 2-(4-bromophenoxy)-5-chlorobenzaldehyde (82.8 mg, 0.3 mmol), CuCl(4.05 mg, 0.03 mmol), and NFSI (189 mg, 0.6 mmol) were added to a 15 mL thick-walled pressure-resistant reaction tube , and 3 mL of acetonitrile was added as solvent. The reaction mixture was magnetically stirred at 100 °C for 24 hours. After completion of the reaction, it was cooled to room temperature, 10 mL of water was added and extracted with dichloromethane (3 x 10 mL). The organic phases were combined and dried with anhydrous NaSO After filtration, the product was purified by column chromatography using petroleum ether/ethyl acetate (20:1, v/v) as eluent. The eluate containing the product was collected and evaporation of the solvent gave 2-bromo-9H-xanthen-9-one as a white solid in 70% yield.

References[1] Organic Letters, 2012, vol. 14, # 3, p. 902 - 905
[2] Patent: CN107641111, 2018, A. Location in patent: Paragraph 0066; 0067; 0068
[3] Organic Letters, 2013, vol. 15, # 4, p. 928 - 931
[4] Organic and Biomolecular Chemistry, 2017, vol. 15, # 7, p. 1589 - 1592
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