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9-Fluorenone-2-carboxylic acid

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9-Fluorenone-2-carboxylic acid Basic information

Product Name:
9-Fluorenone-2-carboxylic acid
Synonyms:
  • 9-Oxo-2-fluorenecarboxyic Acid
  • 9-FLUOROENONE-2-CARBOXYLIC ACID
  • 9-Fluorenone-2-CarboxylicAcid99%
  • 9-Fluorenone-2-Carboxylic Acid 99%
  • 9-Oxofluorene-2-carboxylic acid
  • 9-oxo-2-fluorenecarboxylate
  • 9-Fluorenone-2-carboxylic acid,97%
  • 9-Fluorenone-2-carboxylic acid,9-Oxo-2-fluorenecarboxylic acid
CAS:
784-50-9
MF:
C14H8O3
MW:
224.21
EINECS:
212-317-3
Product Categories:
  • Fluorenes, Flurenones
  • Carboxylic Acids
  • Fluorescent Labels and Indicators
  • Fluorenes & Fluorenones
  • Fluorenones
  • Fluorescent Labels & Indicators
  • Carboxylic Acids
  • Fluorene Derivatives
  • Building Blocks
  • C13 to C42+
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Fused Ring Systems
Mol File:
784-50-9.mol
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9-Fluorenone-2-carboxylic acid Chemical Properties

Melting point:
>300 °C (lit.)
Boiling point:
325.61°C (rough estimate)
Density 
1.2337 (rough estimate)
refractive index 
1.5400 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
form 
Fine Powder
pka
3.85±0.20(Predicted)
color 
Yellow
CAS DataBase Reference
784-50-9(CAS DataBase Reference)
NIST Chemistry Reference
9-Fluorenone-2-carboxylic acid(784-50-9)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29183000

MSDS

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9-Fluorenone-2-carboxylic acid Usage And Synthesis

Chemical Properties

yellow fine powder

Uses

9-Fluorenone-2-carboxylic Acid (cas# 784-50-9) is a compound useful in organic synthesis.

Synthesis Reference(s)

Journal of the American Chemical Society, 70, p. 3958, 1948 DOI: 10.1021/ja01191a530
Organic Syntheses, Coll. Vol. 3, p. 420, 1955

Synthesis

3096-44-4

784-50-9

General procedure for the synthesis of 9-fluorenone-2-carboxylic acid from the compound (CAS: 3096-44-4): potassium hydroxide (1.6 g, 29.4 mmol) was added to a mixture of methanol (7 mL) and water (7 mL) containing compound 12 (200 mg, 0.98 mmol), and the reaction mixture was stirred for 6 hours at 110 °C. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure. The pH was adjusted to 3 with 1 N hydrochloric acid and the mixture was extracted with ethyl acetate (30 mL x 3). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated to afford the target product 9-fluorenone-2-carboxylic acid (200 mg, 91% yield) as a yellow solid.1H NMR (400 MHz, DMSO-d6) δ 13.30 (s, 1H), 8.19 (d, J = 7.6 Hz, 1H), 8.03 (s, 1H), 7.97-9.89 ( m, 2H), 7.72-7.64 (m, 2H), 7.50-7.44 (m, 1H).

References

[1] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 22, p. 5861 - 5872
[2] Patent: CN104557862, 2017, B. Location in patent: Paragraph 0102-0104; 0109-0110

9-Fluorenone-2-carboxylic acid Preparation Products And Raw materials

Raw materials

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