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5,6-Dimethoxy-1-indanone

Names

[ CAS No. ]:
2107-69-9

[ Name ]:
5,6-Dimethoxy-1-indanone

[Synonym ]:
1H-Inden-1-one, 2,3-dihydro-5,6-dimethoxy-
5,6-Dimethoxy-2,3-dihydro-1H-inden-1-on
EINECS 218-287-8
MFCD00612461
5,6-Dimethoxy-indan-1-one
1H-Inden-1-one,2,3-dihydro-5,6-dimethoxy
5,6-dimethoxy-2,3-dihydro-1H-inden-1-one
5,6-dimethoxyindan-1-one
5,6-Dimethoxy-1-indanone
3,4-dimethoxy-1-indanone
5,6-Dimethoxyindan-1-on
5,6-DIMETHOXY-2,3DIHYDRO-1H-INDEN-1-ONE
Donepezil Impurity 25

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
339.7±42.0 °C at 760 mmHg

[ Melting Point ]:
118-122 ºC

[ Molecular Formula ]:
C11H12O3

[ Molecular Weight ]:
192.211

[ Flash Point ]:
150.4±14.3 °C

[ Exact Mass ]:
192.078644

[ PSA ]:
35.53000

[ LogP ]:
2.26

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.550

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914509090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2914509090

[ Summary ]:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Thienylhalomethylketones: Irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools

Bioorg. Med. Chem. 17 , 6914-25, (2009)

Thienylhalomethylketones, whose chemical, biological, and pharmaceutical data are here reported, are the first irreversible inhibitors of GSK-3beta described to date. Their inhibitory activity is like...

Ring-substituted 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides with similar patterns of cytotoxicity to the dual topo I/II inhibitor DACA.

Bioorg. Med. Chem. 7(12) , 2801-9, (1999)

A series of ring-substituted analogues of the topoisomerase inhibitor 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides was prepared and evaluated. The compounds were prepared by Pfitzinger reaction of...

Inhibition of bovine viral diarrhea virus RNA synthesis by thiosemicarbazone derived from 5,6-dimethoxy-1-indanone.

J. Virol. 85(11) , 5436-45, (2011)

In the present work, we described the activity of the thiosemicarbazone derived from 5,6-dimethoxy-1-indanone (TSC), which we previously characterized as a new compound that inhibits bovine viral diar...


More Articles


Related Compounds

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