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6-Phthalazinecarboxylic acid, 3,4-dihydro-1-(hydroxymethyl)-5,7-dimethyl-3-(3-methylphenyl)-4-oxo-, ethyl ester is a complex organic compound with the chemical formula C18H19NO4. It is a derivative of phthalazine, a heterocyclic aromatic compound consisting of a benzene ring fused to a diazine ring. This specific compound features a 3,4-dihydro-phthalazine core with a hydroxymethyl group at position 1, two methyl groups at positions 5 and 7, a 3-methylphenyl group at position 3, and a 4-oxo group. The ethyl ester functional group is attached to the 6-carboxylic acid position, which is a key structural feature of this molecule. 6-Phthalazinecarboxylic acid, 3,4-dihydro-1-(hydroxymethyl)-5,7-dimethyl-3-(3-methylphenyl)-4-oxo-, ethyl ester is known for its potential applications in pharmaceuticals and as an intermediate in the synthesis of various chemical compounds.

73726-38-2

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73726-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73726-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,2 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73726-38:
(7*7)+(6*3)+(5*7)+(4*2)+(3*6)+(2*3)+(1*8)=142
142 % 10 = 2
So 73726-38-2 is a valid CAS Registry Number.

73726-38-2Downstream Products

73726-38-2Relevant academic research and scientific papers

Synthesis and inhibitory effects on platelet aggregation of phthalazinone derivatives

Sugimoto,Ito,Eguchi,et al.

, p. 223 - 228 (2007/10/02)

7-Ethoxycarbonyl-4-hydroxymethyl-6,8-dimethyl-2-phenyl-1(2H)-phthalazinon e 7a and its derivatives having various substituents on the benzene ring at the 2 position were prepared and their inhibitory activities on platelet aggregation were assayed. The parent compound and those having an ortho substituent such as fluorine, chlorine atom or a methyl group showed the most potent inhibitory activity. Their inhibitory mechanism on platelet aggregation was assumed to be inhibition of cyclooxygenase, resulting in prevention of prostaglandin synthesis.

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