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2,3-DIHYDRO-2,2-DIMETHYL-4-METHOXY-1H-INDEN-1-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99545-62-7

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99545-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99545-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,4 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99545-62:
(7*9)+(6*9)+(5*5)+(4*4)+(3*5)+(2*6)+(1*2)=187
187 % 10 = 7
So 99545-62-7 is a valid CAS Registry Number.

99545-62-7Relevant academic research and scientific papers

BICYCLIC BENZENOID ALKYLENE AMINO THIENO[3,4-D]ISOTHIAZOLE ETHERS AND THIOETHERS, PHARMACEUTICAL COMPOSITIONS AND USE

-

, (2015/07/22)

A class of bicyclic benzenoid aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.

BICYCLIC BENZENOID AMINOALKYLENE ETHERS AND THIOETHERS, PHARMACEUTICAL COMPOSITIONS AND USE

-

, (2015/07/22)

A class of bicyclic benzenoid aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.

BICYCLIC BENZENOID AMINOALKYLENE ETHERS AND THIOETHERS, PHARMACEUTICAL COMPOSITIONS AND USE

-

, (2008/06/13)

A class of bicyclic benzenoid aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.

Syntheses of 5-, 7-, and 8-Methoxy-3-methyl-2-tetralone

Johansson, Anette M.,Mellin, Charlotta,Hacksell, Uli

, p. 5252 - 5258 (2007/10/02)

Two efficient syntheses of 5-methoxy- and 8-methoxy-3-methyl-2-tetralone and the synthesis of the 7-methoxy isomer via a different route are described.Also reported is the synthesis of 8-methoxy-3,3-dimethyl-2-tetralone.The regioselectivity of lithium carbanion formation in 1,6-, 1,7-, and 2,7-dihydroxynaphthalene is discussed.The latter compound undergoes dimetalation more easily than the other isomers.

Total Synthesis of Methyl 8-Methoxy-2,2-dimethyl-7-oxo-1,2,3,5,6,7-hexahydro-s-indacen-4-carboxylate: A Key Intermediate for the Synthesis of Illudinine

Ghosh, Anuradha,Dutta, Phanindra Chandra

, p. 2724 - 2747 (2007/10/02)

A simple regioselective synthesis of the title compound (3), an established intermediate for the synthesis of illudinine and the related compounds has been achieved from 7-methoxyindan-1-one (8b) through 4-methoxy-2,2-dimethyl-1,2,3,6,7,8-hexahydrobenzinden-9-one (25) in 13 steps.

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