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(1E)-bis(thiophen-3-ylmethylidene)hydrazine is a hydrazone derivative chemical compound, characterized by two thiophene rings connected by a hydrazine linker. This versatile molecule is known for its potential as a ligand in the synthesis of coordination compounds and its applications in the preparation of heterocyclic compounds. Its molecular structure and properties have garnered interest for its possible biological activities, such as anti-cancer and anti-inflammatory effects, making it a promising candidate for further research and development in both material science and pharmaceuticals.

17303-96-7

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17303-96-7 Usage

Uses

Used in Organic Chemistry:
(1E)-bis(thiophen-3-ylmethylidene)hydrazine is used as a potential ligand for the synthesis of coordination compounds, which are essential in various chemical and catalytic processes. Its unique structure allows for the creation of stable complexes with metal ions, facilitating reactions and improving outcomes in organic synthesis.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1E)-bis(thiophen-3-ylmethylidene)hydrazine is explored for its potential biological activities. It is studied for its anti-cancer properties, where it may contribute to the development of new drugs targeting cancer cells. Additionally, its anti-inflammatory potential is of interest for the treatment of various inflammatory conditions.
Used in Heterocyclic Compound Preparation:
(1E)-bis(thiophen-3-ylmethylidene)hydrazine is utilized in the preparation of heterocyclic compounds, which are important in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its role in creating diverse heterocyclic structures makes it a valuable component in expanding the scope of available compounds for various applications.
Used in Material Science:
(1E)-bis(thiophen-3-ylmethylidene)hydrazine's molecular structure and properties also make it a versatile component in the development of new materials. Its potential use in material science includes the creation of novel polymers, sensors, and other advanced materials that can be tailored for specific applications, such as in electronics or environmental technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 17303-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17303-96:
(7*1)+(6*7)+(5*3)+(4*0)+(3*3)+(2*9)+(1*6)=97
97 % 10 = 7
So 17303-96-7 is a valid CAS Registry Number.

17303-96-7Downstream Products

17303-96-7Relevant academic research and scientific papers

THERMOLYSIS OF SODIUM SALTS OF TOSYLHYDRAZONES OF SOME HETEROCYCLIC ALDEHYDES IN THE PRESENCE OF SILVER CHROMATE: 1,3 NC MIGRATION OF TOSYL GROUP

Saito, Katsuhiro,Ishihara, Hiraku

, p. 1891 - 1898 (2007/10/02)

The thermal decompositions of sodium salts of tosylhydrazones of furfural, thiophene-2-aldehyde, 1-methylpyrrole-2-aldehyde, and pyridine-2-aldehyde in the presence of silver chromate gave 2-furyl(p-toluenesulfonyl)methane, thiophene-2-(p-toluenesulfonyl)methane, 1-methylpyrrole-2-(p-toluenesulfonyl)methane, and pyridine-2-(p-toluenesulfonyl)methane, respectively, via 1,3 NC migration of tosyl group.The same type of reactions with sodium salts of tosylhydrazones of thiophene-3-aldehyde, pyridine-3-aldehyde, and pyridine-4-aldehyde also afforded the corresponding p-toluenesulfonylmethanes but the yields were slightly lower comparing to the above cases.

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