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6-Aminoindanone

Basic information Uses Safety Supplier Related

6-Aminoindanone Basic information

Product Name:
6-Aminoindanone
Synonyms:
  • 6-AMINO-1-INDANONE
  • 6-AMINO-INDAN-1-ONE
  • 6-AMINOINDANONE
  • 6-Amino-2,3-dihydro-1H-inden-1-one
  • 1H-Inden-1-one, 6-amino-2,3-dihydro-
  • 6-AMino-1-oxoindane
  • 6-Amino-2,3-dihydro-1H-inden-1-one, 6-Amino-2,3-dihydro-1-oxo-1H-indene
  • 6-Amino-1-indenone
CAS:
69975-65-1
MF:
C9H9NO
MW:
147.17
Product Categories:
  • Indanone & Indene
Mol File:
69975-65-1.mol
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6-Aminoindanone Chemical Properties

Melting point:
167-171 °C(Solv: methanol (67-56-1))
Boiling point:
330.3±31.0 °C(Predicted)
Density 
1.254±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Solution
pka
3.85±0.20(Predicted)
color 
Light brown to black
InChI
InChI=1S/C9H9NO/c10-7-3-1-6-2-4-9(11)8(6)5-7/h1,3,5H,2,4,10H2
InChIKey
UOJCPAAEKXNPQT-UHFFFAOYSA-N
SMILES
C1(=O)C2=C(C=CC(N)=C2)CC1
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
2811
HazardClass 
IRRITANT
PackingGroup 
HS Code 
29223900
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6-Aminoindanone Usage And Synthesis

Uses

6-Amino-1-indanone is a synthetic compound belonging to the indanone class. It is an ethylene oxide synthesized via a multi-step process involving the dehydration and reductive amination of an amine. In organic chemistry, it is used as an intermediate in the synthesis of various other compounds, such as serotonin. This compound exhibits an affinity for palladium catalysts during reductive amination, which can be used for sequence optimization experiments.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 46, p. 399, 2003 DOI: 10.1021/jm020067s

Synthesis

24623-24-3

69975-65-1

The general procedure for the synthesis of 6-amino-1-indanone from 6-nitro-1-indanone was as follows: a mixed suspension of 6-nitroindan-1-one (10 g, 56 mmol) with 10% Pd/C catalyst (2.0 g) in methanol (200 mL) was subjected to stirring in a hydrogenation reactor for 3 hr at room temperature under a hydrogen pressure of 30 psi. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to afford 6-aminoindan-1-one (7.2 g, 87% yield).

References

[1] Chemistry - A European Journal, 2015, vol. 21, # 37, p. 13052 - 13057
[2] Patent: WO2006/71940, 2006, A2. Location in patent: Page/Page column 396
[3] Patent: WO2007/148808, 2007, A1. Location in patent: Page/Page column 126-127
[4] Journal of Medicinal Chemistry, 2003, vol. 46, # 3, p. 399 - 408
[5] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 20, p. 5665 - 5670

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