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2-Acetonilidene-3,4-diphenyl-2,3-dihydrothiazole is a complex organic compound characterized by a unique molecular structure. It features a thiazole ring, which is a five-membered heterocyclic ring containing sulfur and nitrogen. The compound is further distinguished by the presence of a 2-acetonilidene group, which is a ketone derivative, and two phenyl groups attached to the 3 and 4 positions of the thiazole ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its diverse functional groups and stable ring structure. The compound's properties, such as its reactivity and stability, make it a valuable intermediate in organic synthesis, particularly in the development of new drugs and materials.

3364-97-4

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3364-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3364-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3364-97:
(6*3)+(5*3)+(4*6)+(3*4)+(2*9)+(1*7)=94
94 % 10 = 4
So 3364-97-4 is a valid CAS Registry Number.

3364-97-4Downstream Products

3364-97-4Relevant academic research and scientific papers

Utility involving thioacetoacetanilides as precursors for synthesis of new thiazole, thiadiazole and thiophene derivatives with antimicrobial activity

Fekri, Ahmed,Keshk, Eman M.

, p. 148 - 161 (2016/03/26)

The behavior of thioacetoacetanilide (1) and/or α-arylhydrazono-thioacetoacetanilides 4 toward many different α-halocarbonyl compounds was demonstrated. Thus, reactions of 1 with α-bromoketones (bromoacetone and phenacyl bromide) and hydrazonoyl bromides

Synthesis and Heterocyclization of 3-Arylaminothiocrotonanilides

Borisevich, A. N.,Samoilenko, L. S.,Lozinskii, M. O.,Rusanov, E. B.,Chernega, A. N.

, p. 1767 - 1770 (2007/10/03)

Reactions of acetylthioacetanilide with arylamines in acetic acid in the presence of sodium acetate give 3-arylaminothiocrotonanilides in good yields. When treated with ω-bromoacetophenone in acetone, these products are converted to substituted 4-hydroxy-

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