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4-(3,4-dimethyl-phenyl)-2H-phthalazin-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93517-74-9

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93517-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93517-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,1 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93517-74:
(7*9)+(6*3)+(5*5)+(4*1)+(3*7)+(2*7)+(1*4)=149
149 % 10 = 9
So 93517-74-9 is a valid CAS Registry Number.

93517-74-9Relevant academic research and scientific papers

POTASSIUM CHANNEL MODULATORS

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Page/Page column 43-44, (2011/06/19)

Disclosed herein are KCNQ potassium channels modulators of formula (I) wherein ring Z1, R1, p, R3, and R4 are as defined in the specification. Compositions comprising such compounds; and methods for treating conditions and disorders using such compounds and compositions are also described.

Synthesis and anti-inflammatory evaluation of some condensed [4-(3,4-dimethylphenyl)-1(2H)-oxo-phthalazin-2-yl]acetic acid hydrazide

Abd alla, Mosaad S.M.,Hegab, Mohamed I.,Abo Taleb, Nageh A.,Hasabelnaby, Sherifa M.,Goudah

experimental part, p. 1267 - 1277 (2010/06/12)

Some new 1,3,4-triazolo-, 1,3,4-oxadiazolo-, 1,3,4-thiadiazol-, and pyrazolo-3,4-dimethylphenyl-1(2H)-oxo-phthalazine derivatives were synthesized and identified by IR, 1H NMR, MS and elemental analysis. Most of the newly synthesized products were tested for their anti-inflammatory activities. Among them, compounds 11, 17b, 20, 21 and 22 are active compare to the activity of indomethacin.

Synthesis and some reactions of 3,4-dimethoxyphenylmethyleneaminophthalimide

Derbala, H. A. Y.

, p. 779 - 781 (2007/10/02)

3,4-Dimethoxyphenylmethyleneaminophthalimide (1) reacts with aromatic hydrocarbons under Friedel-Craft's conditions to give 4-arylphthalazin-1-ones (2a-c).The reaction involves ring cleavage followed by cyclization and elimination of the aldehyde moiety.The investigation is extended to study the reaction of the title compound with Grignard reagents and amines leading to the formation of 2a, 4-6), respectively.

REACTIONS OF 2,3-DIARYL-3-HYDROXYPHTHALIMIDINES WITH GRIGNARD REAGENTS AND HYDRAZINE HYDRATE

Ismail, Mohamed Fekry,Enayat, Ebtesam Ismail,El-Bassiouny, Fakhry Abdel Aziz,Younes, Hamed Ahmed

, p. 677 - 678 (2007/10/02)

2,3-diaryl-3-hydroxyphthalimidines, 1, react with benzylmagnesium chloride to give 3-aryl-3-benzylphthalides 2.The reaction involves the removal of the amine part at position 2.Reaction of 1a with phenylmagnesium bromide proceeded differently to give 3.Th

NEW CONVENIENT ONE-STEP SYNTHESIS OF 4-ARYLPHTHALAZ-1-ONES

Ismail, M. Fekry,El-Bassiouny, F. A.,Younes, H. A.

, p. 2983 - 2984 (2007/10/02)

4-Arylphthalaz-1-ones (2a-e) are prepared by the hitherto unknown reaction of N-aminophthalimide (1) with aromatic hydrocarbons under Friedel-Crafts conditions.The reaction of N-aminophthalimide with Grignard reagents presents another convenient method for the synthesis of 4-alkyl or 4-arylphthalaz-1-ones.

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