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(4-Methoxyphenyl)-(1-phthalimidoethyl)-keton is a complex organic compound with the molecular formula C17H13NO4. It is characterized by a ketone group, which is a carbonyl group (C=O) bonded to two carbon atoms. The compound features a 4-methoxyphenyl group, which is a phenyl ring (a six-carbon aromatic ring) with a methoxy (-OCH3) substituent at the 4-position. Additionally, it has a 1-phthalimidoethyl group, which is an ethyl chain (-CH2CH2-) attached to a phthalimide ring (a cyclic imide derived from phthalic anhydride). This chemical is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

19427-11-3

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19427-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19427-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,2 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19427-11:
(7*1)+(6*9)+(5*4)+(4*2)+(3*7)+(2*1)+(1*1)=113
113 % 10 = 3
So 19427-11-3 is a valid CAS Registry Number.

19427-11-3Relevant academic research and scientific papers

Antimitotic agents. Chiral isomers of ethyl [5-amino-1,2-dihydro-3-(4- hydroxyphenyl)-2-methylpyrido[3,4-b]pyrazin-7-yl]carbamate

Temple Jr.,Rener

, p. 988 - 993 (2007/10/02)

Metabolism studies with ethyl [5-amino-1,2-dihydro-2-methyl-3- phenylpyrido[3,4-b]pyrazin-7-yl]carbamate (1) in mice were reported previously to give a hydroxylated metabolite, which was methylated to give a methoxy derivative. The metabolite and its deri

Ferric Chloride-Catalyzed Acylation of Aromatic Compounds with N-Phthaloyl-α-amino Acyl Chlorides without Racemisation

Effenberger, Franz,Steegmueller, Dieter

, p. 117 - 124 (2007/10/02)

Reactive aromatic compounds are acylated without racemisation to aryl 1-phthalimidoalkyl ketones 4 in good yields with N-phthaloyl-α-amino acid chlorides in the presence of catalytic amounts (1 to 5 mol-percent) of FeCl3.This new method is especially useful for the synthesis of the pharmacologically interesting alkoxyaryl 1-phthalimidoalkyl ketones 6, 8, 10, and 11, which cannot be prepared in reasonable yields in the presence of other FC catalysts such as AlCl3 or SnCl4.

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