9-Fluorenone-2-carboxylic acid
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
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)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29183000
MSDS
- Language:English Provider:9-Fluorenone-2-carboxylic acid
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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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9-Fluorenone-2-carboxylic acid(784-50-9)Related Product Information
- Glycine
- Ethyl 2-(Chlorosulfonyl)acetate
- Folic acid
- 9-Fluorenone
- Phenylfluorone
- 2,5-Dimethylbenzaldehyde
- 4-Phenyltoluene
- 3'-Methylacetophenone
- 3-Methylbenzophenone
- 3-Methylbenzyl alcohol
- 2-FLUORENECARBOXALDEHYDE
- 3,4-Dimethylbenzaldehyde
- Benzophenone
- 3-Ethylbenzaldehyde
- 2',5'-DIMETHYLACETOPHENONE
- 3,4-Dimethylbenzoic acid
- 9-FLUORENONE-2,7-DICARBOXYLIC ACID
- toluic acid