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2-INDANCARBOXYLIC ACID

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2-INDANCARBOXYLIC ACID Basic information

Product Name:
2-INDANCARBOXYLIC ACID
Synonyms:
  • 2-INDANCARBOXYLIC ACID
  • 2-INDANECARBOXYLIC ACID
  • CBI-BB ZERO/005363
  • INDAN-2-CARBOXYLIC ACID
  • Indancarboxylicacid
  • 2-INDANCARBOXYLIC ACID 98+%
  • TIMTEC-BB SBB003945
  • 2-Carboxyindane
CAS:
25177-85-9
MF:
C10H10O2
MW:
162.19
Product Categories:
  • C10
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
25177-85-9.mol
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2-INDANCARBOXYLIC ACID Chemical Properties

Melting point:
128-132 °C (lit.)
Boiling point:
192 °C / 18mmHg
Density 
1.0281 (rough estimate)
refractive index 
1.6000 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
pka
4.65±0.20(Predicted)
form 
Crystalline Powder
color 
White to cream or brown
CAS DataBase Reference
25177-85-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29163990

MSDS

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2-INDANCARBOXYLIC ACID Usage And Synthesis

Chemical Properties

White powder

Synthesis

26453-01-0

25177-85-9

General procedure for the synthesis of 2-indenecarboxylic acid from 2,3-dihydro-1H-indene-2-carbonitrile: A mixture of 2,3-dihydro-1H-indene-2-carbonitrile (128) (55.1 g, 0.385 mol), concentrated hydrochloric acid (100 mL), and dioxane (500 mL) was stirred for 41 hours at 60-70°C. Upon completion of the reaction, the mixture was cooled and the dioxane was removed by evaporation to give a residue. The residue was suspended in 1 M hydrochloric acid (300 mL) and stirred at 20 °C for 15 hours. Subsequently, the solid product was collected by filtration, washed with water and dried to give 2-indenecarboxylic acid (129) (54.1 g, 87% yield) as a white solid. Melting point (EtOAc/petroleum ether recrystallization) 128 °C [literature value (Baeyer, A. Perkin W.H., Chem. Ber. 1884, 17, 122) mp 130.2 °C]; 1H NMR (δ): 10.50 (broad single peak, 1H, COOH), 7.14-7.25 (multiple peaks, 4H, H-4, H-5, H -6, H-7), 3.21-3.43 (multiple peaks, 5H, H-1, H-2, H-3).

References

[1] Patent: WO2006/104406, 2006, A1. Location in patent: Page/Page column 112
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 21, p. 6853 - 6865

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