ChemicalBook--->CAS DataBase List--->6342-80-9

6342-80-9

6342-80-9 Structure

6342-80-9 Structure
IdentificationBack Directory
[Name]

4,5-DIMETHOXY-1-INDANONE
[CAS]

6342-80-9
[Synonyms]

4,5-DIMETHOXY-1-INDANONE
4,5-DIMETHOXY-INDAN-1-ONE
4,5-Dimethoxy-1-indanone 97%
4,5-dimethoxy-2,3-dihydroinden-1-one
4,5-DiMethoxy-2,3-dihydro-1H-inden-1-one
2,3-dihydro-4,5-dimethoxy-1H-Inden-1-one
1H-Inden-1-one, 2,3-dihydro-4,5-diMethoxy-
[Molecular Formula]

C11H12O3
[MDL Number]

MFCD00463187
[MOL File]

6342-80-9.mol
[Molecular Weight]

192.21
Chemical PropertiesBack Directory
[Melting point ]

73-77 °C (lit.)
[Boiling point ]

160-161 °C(Press: 2 Torr)
[density ]

1.179±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

4,5-Dimethoxy-1-indanone acts as a reagent for the preparation of thiosemicarbazones derived from 1-indanone as new anti-trypanosoma cruzi agents.
[Definition]

ChEBI: 4,5-dimethoxy-2,3-dihydroinden-1-one is a member of indanones.
[Synthesis]

3-(2,3-DIMETHOXYPHENYL)PROPANOIC ACID

10538-48-4

4,5-DIMETHOXY-1-INDANONE

6342-80-9

3-(2,3-dimethoxyphenyl)propionic acid (4.99 g, 23.7 mmol) was mixed with Eaton's reagent (47.5 mL, 3 g/mmol of raw material) and stirred at room temperature for 72 hours. Upon completion of the reaction, the mixture was slowly poured into ice water, neutralized to neutral, and subsequently extracted with ethyl acetate (3 x 75 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by fast column chromatography using a pre-packed 100 g silica gel column [eluent A: ethyl acetate; eluent B: n-hexane; gradient elution: 7% A/93% B (1 column volume), 7% A/93% B→60% A/40% B (10 column volumes), 60% A/40% B (2 column volumes); flow rate: 40 mL/min; detection wavelengths: 254 nm and 280 nm] to give 4,5-dimethoxy-1-indanone (2.01 g, 10.5 mmol, 44% yield) as a yellow solid.1H NMR (CDCl3, 600 MHz) δ 7.06 (1H, d, J = 8.4 Hz), 6.62 (1H, d, J = 8.4 Hz), 3.61 (3H, s), 3.57 (3H, s), 2.70 (2.70 (2.70), 2.70 (2.70), 2.70 (2.70), 2.70 (3H, s), 2.70 (3H, s). s), 2.70 (2H, t, J = 5.4 Hz), 2.25 (2H, t, J = 5.4 Hz).13C NMR (CDCl3, 150 MHz) δ 204.6, 157.1, 147.4, 145.0, 130.7, 119.4, 112.0, 59.8, 55.8, 36.0, 22.1.

[References]

[1] Canadian Journal of Chemistry, 1982, vol. 60, # 21, p. 2678 - 2686
[2] Synthetic Communications, 2001, vol. 31, # 13, p. 2029 - 2036
[3] Journal of Medicinal Chemistry, 2011, vol. 54, # 9, p. 3331 - 3347
[4] Journal of Medicinal Chemistry, 1987, vol. 30, # 8, p. 1303 - 1308
[5] Journal of Organic Chemistry, 1984, vol. 49, # 12, p. 2130 - 2135
Spectrum DetailBack Directory
[Spectrum Detail]

4,5-DIMETHOXY-1-INDANONE(6342-80-9)1HNMR
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