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2H-Indol-2-one, 1,3-dihydro-1-[(4-methoxyphenyl)amino]-3-phenyl- is a complex organic compound with the chemical formula C20H18N2O2. It is a derivative of indole-2-one, featuring a 1,3-dihydro structure, which means it has two hydrogen atoms added across the double bond between carbons 1 and 3. The compound is characterized by the presence of a 4-methoxyphenyl group attached to the nitrogen atom at position 1, and a phenyl group at position 3. This molecule is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting various biological pathways. Its structure and properties make it a subject of interest for chemists and biologists studying the interactions of such compounds with biological systems.

79006-03-4

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79006-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79006-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79006-03:
(7*7)+(6*9)+(5*0)+(4*0)+(3*6)+(2*0)+(1*3)=124
124 % 10 = 4
So 79006-03-4 is a valid CAS Registry Number.

79006-03-4Relevant academic research and scientific papers

CONVERSIONS OF 1-ARYLAMINO-3-PHENYLOXINDOLES

Glushkov, V. A.,Berdinskii, I. S.,Gartman, G. A.

, p. 1119 - 1122 (1984)

Acylation of 1-arylamino-3-phenyloxindoles by acetic anhydride in the presence of an acidic catalyst (TsOH) gives N-acetyl derivatives; alkylation by methyl iodide in the presence of sodium ethoxide gives C(3)- and N-dimethyl derivatives.Reduct

1-Arylamino-3-phenyl-2,3-dihydro-2-indolones

Glushkov, V. A.,Berdinskii, I. S.

, p. 349 - 351 (2007/10/02)

α-Chlorodiphenylacetyl chloride reacts with arylhydrazines to give 1-arylamino-3-phenyl-2,3-dihydro-2-indolones, which undergo acetylation at the nitrogen and oxygen and undergo benzoylation at the nitrogen atom.

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