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CARBAZOL-9-YL-ACETIC ACID

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CARBAZOL-9-YL-ACETIC ACID Basic information

Product Name:
CARBAZOL-9-YL-ACETIC ACID
Synonyms:
  • TIMTEC-BB SBB010077
  • CARBAZOL-9-YL-ACETIC ACID
  • 9-CARBAZOLEACETIC ACID
  • (9-carbazolyl)acetic acid
  • (9-Carbazolyl)acetic acid, 9-(Carboxymethyl)carbazole
  • 9-Carbazoleacetic acid, ≥99.0% (T)
  • 2-(9-carbazolyl)acetic acid
  • 2-(9H-Carbazole-9-yl)acetic acid
CAS:
524-80-1
MF:
C14H11NO2
MW:
225.24
Mol File:
524-80-1.mol
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CARBAZOL-9-YL-ACETIC ACID Chemical Properties

Melting point:
191-194 °C
Boiling point:
366.75°C (rough estimate)
Density 
1.1508 (rough estimate)
refractive index 
1.5780 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
3.13±0.10(Predicted)
Appearance
White to off-white Solid
Merck 
13,1798
BRN 
190299
InChIKey
PBDMLLFEZXXJNE-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT

MSDS

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CARBAZOL-9-YL-ACETIC ACID Usage And Synthesis

Synthesis

86-74-8

105-36-2

524-80-1

The general procedure for the synthesis of 9-carbazoleacetic acid from carbazole and ethyl bromoacetate was as follows: 5 g (0.03 mol) of carbazole was dissolved in 100 mL of DMF, followed by the addition of 6.68 g (0.04 mol) of ethyl bromoacetate. The reaction mixture was stirred continuously at 35 °C for 12 hours. After completion of the reaction, the mixture was poured into 200 mL of water and separated by filtration. The pH of the filtrate was adjusted to 1.0 with 2 M hydrochloric acid. the crude product was collected by filtration and dried. The crude product was recrystallized by dichloromethane/ethanol solvent mixture to give 6.1 g of white crystalline product in 90% yield. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz, δ ppm) and 13C NMR (DMSO-d6, 100 MHz, δ ppm): 1H NMR showed δ 13.10 (s, 1H), 8.16 (d, 2H, J = 7.8 Hz), 7.55 (m, 2H), 7.42 (m, 2H), 7.22 ( m, 2H), 5.23 (s, 2H); 13C NMR showed δ 170.2, 140.4, 125.6, 122.2, 120.1, 119.0, 109.2, 43.9.

Purification Methods

Crystallise the acid from ethyl acetate. [Fan et al. Anal Chim Acta 367 1 1998, Beilstein 20 III/IV 3841.]

References

[1] Tetrahedron, 2014, vol. 70, # 14, p. 2478 - 2486
[2] Organic Preparations and Procedures International, 2000, vol. 32, # 3, p. 284 - 287

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