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2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole is a heterocyclic chemical compound characterized by the presence of a thiadiazole ring with a chloromethyl and ethoxy substituent. It is known for its unique structural properties and reactivity, making it a valuable building block in organic chemistry and drug discovery. 2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole holds potential for various biological activities, which positions it as a promising target for research and development in different fields.

4153-74-6

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4153-74-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with unique therapeutic properties. Its reactivity allows for the creation of diverse chemical entities that can target specific biological pathways.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its incorporation can enhance the effectiveness of these products, leading to improved crop protection and yield.
Used in Organic Chemistry Research:
2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole serves as a versatile building block in organic chemistry, facilitating the exploration of novel chemical reactions and the synthesis of complex organic compounds. Its unique structure allows researchers to investigate new pathways and mechanisms in chemical synthesis.
Used in Drug Discovery:
2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole is employed as a starting material in drug discovery processes, where its potential biological activities are explored for the development of new therapeutic agents. Its heterocyclic nature provides a foundation for the design of molecules with specific pharmacological properties.
While the exact uses and properties of 2-(chloromethyl)-5-ethoxy-1,3,4-thiadiazole may vary depending on the specific application and formulation, its diverse applications across industries highlight its significance in modern chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 4153-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4153-74:
(6*4)+(5*1)+(4*5)+(3*3)+(2*7)+(1*4)=76
76 % 10 = 6
So 4153-74-6 is a valid CAS Registry Number.

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