6-Nitrochroman-4-one

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6-Nitrochroman-4-one manufacturers

  • 6-Nitrochroman-4-one
  • 6-Nitrochroman-4-one pictures
  • $6.68
  • 2020-01-13
  • CAS: 68043-53-8
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 1kg-1000kg
6-Nitrochroman-4-one Basic information
Product Name:6-Nitrochroman-4-one
Synonyms:6-NITROCHROMANONE;6-NITROCHROMAN-4-ONE;6-Nitrochroman-4-one 98%;6-Nitro-4-chromanone;2,3-Dihydro-6-nitro-4H-chromen-4-one, 2,3-Dihydro-6-nitro-4H-1-benzopyran-4-one;6-Nitrochroman-4-one98%;6-Nitro-2,3-dihydrochromen-4-one;4H-1-Benzopyran-4-one, 2,3-dihydro-6-nitro-
CAS:68043-53-8
MF:C9H7NO4
MW:193.16
EINECS:
Product Categories:
Mol File:68043-53-8.mol
6-Nitrochroman-4-one Structure
6-Nitrochroman-4-one Chemical Properties
Melting point 116-119
Boiling point 378.7±42.0 °C(Predicted)
density 1.424±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceLight brown to brown Solid
CAS DataBase Reference68043-53-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2932190090
MSDS Information
6-Nitrochroman-4-one Usage And Synthesis
Synthesis
3-(4-NITROPHENYL)PROPANOIC ACID

10572-16-4

6-Nitrochroman-4-one

68043-53-8

The general procedure for the synthesis of 6-nitro-3,4-dihydrochromanone from 3-(4-nitrophenoxy)propionic acid is as follows: 3-(4-nitrophenoxy)propionic acid (6.5 g, 30 mmol), concentrated sulfuric acid (30 mL), and phosphorus pentoxide (5.2 g, 37 mmol) were mixed, and the reaction was stirred for 3 hours at 60 °C. After the reaction was completed, the mixture was poured into ice and stirring was continued for 15 minutes. Subsequently, extraction was carried out with ethyl acetate and the organic phase was washed with saturated aqueous sodium bicarbonate and dried over anhydrous magnesium sulfate. Finally, the organic phase was concentrated in vacuum to afford 6-nitro-3,4-dihydrochromanone as a beige solid (5.5 g, 94% yield) with a melting point of 171-173 °C. The structure of the product was confirmed by NMR and mass spectrometry.

References[1] Patent: WO2005/37830, 2005, A1. Location in patent: Page/Page column 18
[2] Patent: EP2487171, 2012, A1. Location in patent: Page/Page column 9
[3] Patent: WO2014/418, 2014, A1. Location in patent: Page/Page column 97
[4] Patent: US2015/197511, 2015, A1. Location in patent: Paragraph 0450; 0451
[5] Patent: CN108440404, 2018, A. Location in patent: Paragraph 0075; 0079; 0080; 0081
6-Nitrochroman-4-one Preparation Products And Raw materials
Raw materials3-(4-Nitrophenyl)propanoic acid-->4-Chromanone
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