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Benzaldehyde (4-oxo-3-phenyl-3,4-dihydro-2-quinazolinyl)hydrazone is a complex organic compound with the chemical formula C20H16N4O. It is derived from benzaldehyde, which is an aromatic aldehyde, and 4-oxo-3-phenyl-3,4-dihydro-2-quinazolinyl, a quinazoline derivative. benzaldehyde (4-oxo-3-phenyl-3,4-dihydro-2-quinazolinyl)hydrazone is characterized by its conjugated system, which includes a benzene ring, an aldehyde group, and a quinazoline ring. It is known for its potential applications in the synthesis of various pharmaceuticals and as a building block in organic chemistry. The compound's structure allows for a range of chemical reactions, making it a versatile intermediate in the preparation of more complex molecules. Its properties, such as solubility and reactivity, can be influenced by the presence of the aldehyde and hydrazone functional groups, which can participate in a variety of chemical transformations.

3318-07-8

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3318-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3318-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3318-07:
(6*3)+(5*3)+(4*1)+(3*8)+(2*0)+(1*7)=68
68 % 10 = 8
So 3318-07-8 is a valid CAS Registry Number.

3318-07-8Relevant academic research and scientific papers

A new convenient synthesis of 2,4-disubstituted-1,2,4-triazolo[1,5-a] quinazolin-5(4H)-ones

Shawali, Ahmad S.,Hassaneen, Hamdi M.,Shurrab, Nabil Kh.

experimental part, p. 1825 - 1829 (2009/06/08)

(Chemical Equation Presented) A novel series of 2,4 disubstituted-1,2,4- triazolo[1,5-a]quinazolin-5(4H)-ones were prepared by Dimroth rearrangement of their respective isomers namely 1,4-disubstituted-[1,2,4]triazolo[4,3-a]- quinazolin-5(4H)-ones. The la

Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H-quinazolin-4-one as analgesic, anti-inflammatory agents

Alagarsamy,Raja Solomon,Dhanabal

, p. 235 - 241 (2008/02/02)

A variety of novel 3-phenyl-2-substituted-3H-quinazolin-4-ones were synthesized by reacting the amino group of 2-hydrazino-3-phenyl-3H-quinazolin-4-one with different aldehydes and ketones. The starting material 2-hydrazino-3-phenyl-3H-quinazolin-4-one was synthesized from aniline. The title compounds were investigated for analgesic, anti-inflammatory and ulcerogenic index activities. While the test compounds exhibited significant activity, compounds, 2-(N′-2-butylidene-hydrazino)-3-phenyl-3H-quinazolin-4-one (AS1), 2-(N′-3-pentylidene-hydrazino)-3-phenyl-3H-quinazolin-4-one (AS2) and 2-(N′-2-pentylidene-hydrazino)-3-phenyl-3H-quinazolin-4-one (AS3), exhibited moderate analgesic activity. The compound 2-(N′-2-pentylidene-hydrazino)-3-phenyl-3H-quinazolin-4-one (AS3) showed more potent anti-inflammatory activity when compared to the reference standard diclofenac sodium. Interestingly, the test compounds showed only mild ulcerogenic side effect when compared to aspirin.

Chemistry of Quinazolines: Reinvestigation of the Action of Hydrazine on Thioxo Derivatives

Badawy, Mohamed A.,Abdel-Hady, Sayed A. L.,Ibrahim, Yehia A.,Kadry, Azza M.

, p. 1535 - 1536 (2007/10/02)

The action of hydrazine on 2-mercapto and 2-alkylmercaptoquinazolin-4-ones is reinvestigated.The structure of the isolated products have been revised.

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