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(3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine is a dithiazolamine derivative characterized by its molecular formula C13H10N4S2. This chemical compound features a three-dimensional structure with a thiazole ring and an amino group, and it is known to exist as a yellow solid with a melting point of approximately 237-240°C. Its potential applications span across various fields, including medicinal chemistry and pharmaceutical research, due to its biological activities such as antibacterial and antifungal properties. Furthermore, (3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine has been investigated for its use as a coordination ligand in metal complexes, which could have significant implications for the fields of catalysis and material science.

57633-33-7

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57633-33-7 Usage

Uses

Used in Pharmaceutical Research:
(3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine is used as a compound in pharmaceutical research for its potential antibacterial and antifungal properties. Its unique structure and biological activities make it a promising candidate for the development of new drugs to combat various infections.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine is utilized as a starting material or a building block for the synthesis of more complex molecules with potential therapeutic applications. Its structural features and reactivity can be exploited to design and create novel pharmaceuticals.
Used in Material Science:
(3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine is used as a coordination ligand in material science for the formation of metal complexes. These complexes can exhibit unique catalytic properties, which can be harnessed for various industrial applications, including the development of new catalysts for chemical reactions and the creation of advanced materials with specific properties.
Used in Catalysis:
In the field of catalysis, (3Z)-N-phenyl-3-(phenylimino)-3H-1,2,4-dithiazol-5-amine is employed as a ligand in the synthesis of metal complexes that can act as catalysts. These catalysts can improve the efficiency and selectivity of various chemical reactions, leading to more sustainable and cost-effective processes in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 57633-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57633-33:
(7*5)+(6*7)+(5*6)+(4*3)+(3*3)+(2*3)+(1*3)=137
137 % 10 = 7
So 57633-33-7 is a valid CAS Registry Number.

57633-33-7Relevant academic research and scientific papers

1,3-Dipolar cycloaddition of 3-phenylamino-5-phenylimino-1,2,4-dithiazole to 1-acyl-2-phenylacetylenes - A new route to functionalized 1,3-thiazole derivatives

Glotova,Dvorko,Albanov,Kazheva,Shilov,D'yachenko

experimental part, p. 1532 - 1537 (2009/06/28)

3-Phenylamino-5-phenylimino-1,2,4-dithiazole reacted with 1-acyl-2-phenylacetylenes in ethanol or toluene on heating (78-80°C, 1 h) in chemo- and regioselective fashion to give previously unknown N-[5-acyl-3,4-diphenyl-1,3-thiazol-2(3H)-ylidene]-N′-phenyl

A One-Step Synthesis of 1,5-Disubstituted 2,4-Dithiobiurets and Their Oxidation to 3,5-Di(substitutedimino)-1,2,4-dithiazolidines

Joshua, C. P.,Presannan, E.,Thomas, Saramma K.

, p. 649 - 651 (2007/10/02)

In presence of alkali, 1-substituted thioureas condense with isothiocyanates forming 1,5-disubstituted 2,4-dithiobiurets (2).The structure of the products has been confirmed by chemical as well as spectral studies.Oxidation of 2 yields 3,5-di(substitutedi

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