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2-Butenamide, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-N-phenyl- is a complex organic compound with the chemical formula C17H13ClNO3. It is a derivative of butenamide, featuring a 4-chlorophenyl group, a hydroxyl group, and a phenyl group attached to the 4-oxo-butenamide structure. 2-Butenamide, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-N-phenyl- is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its molecular structure provides a foundation for further chemical modifications, which can lead to the development of new therapeutic agents. The compound's specific properties, such as its reactivity and stability, make it a valuable component in the creation of advanced pharmaceuticals.

85635-70-7

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85635-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85635-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,3 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85635-70:
(7*8)+(6*5)+(5*6)+(4*3)+(3*5)+(2*7)+(1*0)=157
157 % 10 = 7
So 85635-70-7 is a valid CAS Registry Number.

85635-70-7Relevant academic research and scientific papers

Five-Membered 2,3-Dioxoheterocycles. XLII. Bifunctional Catalysis with Phosphinic Acids of Decyclization of 5-Aryl-2,3-Dihydro-2,3-Furandiones under the Action of Arylamines

Kozlov,Sazhnev,Kozlova,Andreichikov

, p. 1523 - 1528 (2007/10/03)

The kinetics of reaction of 5-aryl-2,3-dihydro-2,3-furandiones with aniline and anesthesin catalyzed by phosphinic acids is studies by spectrophotometric method in solvents of different polarity and solvation ability. Analysis of the dependence of the rea

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XLIII. BIFUNCTIONAL CATALYSIS BY CARBOXYLIC ACIDS IN THE OPENING OF THE RING OF 5-ARYL-2,3-DIHYDROFURAN-2,3-DIONES BY THE ACTION OF ANILINE AND N-METHYLANILINE. EFFECT OF SUBSTITUENTS IN THE CATALYST AND

Kozlov, A. P.,Sychev, D. I.,Andreichikov, Yu. S.

, p. 167 - 174 (2007/10/02)

The kinetics of the reactions of 5-aryl-2,3-dihydrofuran-2,3-diones with aniline and N-methylaniline in toluene, catalyzed by carboxylic acids, were studied.By analysis of the dependence of the reaction rate on the nature of the substituents in the carbox

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XLII. RING OPENING IN 5-ARYL-2,3-DIHYDRO-2,3-FURANDIONES BY THE ACTION OF AROMATIC AMINES IN TOLUENE. EFFECT OF SUBSTITUENTS IN THE NUCLEOPHILIC REAGENTS AND SUBSTRATE ON THE RATE OF THE NONCATALYTIC REAC

Kozlov, A. P.,Sychev, D. I.,Andreichikov, Yu. S.

, p. 1965 - 1972 (2007/10/02)

The kinetics of the reactions of 5-aryl-2,3-dihydro-2,3-furandiones with aromatic amines were investigated by a spectrophotometric method.On the basis of an analysis of the dependence of the reaction rate on the nature of the substituents in the substrate

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