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1-(4-Amino-2-ethylamino-thiazol-5-yl)-ethanone is a chemical compound characterized by its thiazole derivative structure, featuring an amino group and an ethylamino group attached to the thiazole ring. With a molecular formula of C9H14N2OS, 1-(4-Amino-2-ethylamino-thiazol-5-yl)-ethanone is recognized for its significance in organic synthesis and pharmaceutical research.

107401-79-6

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107401-79-6 Usage

Uses

Used in Pharmaceutical Research:
1-(4-Amino-2-ethylamino-thiazol-5-yl)-ethanone is utilized as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs. Its unique structure and chemical properties make it a valuable building block for creating complex molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-Amino-2-ethylamino-thiazol-5-yl)-ethanone serves as a key component for constructing more intricate molecules. Its versatile structure allows for the creation of a wide range of compounds with potential applications in various industries.
Used in Materials Science:
Due to its distinct structural features, 1-(4-Amino-2-ethylamino-thiazol-5-yl)-ethanone may also find potential applications in the field of materials science. Its properties could be harnessed to develop novel materials with specific characteristics, such as improved stability or enhanced reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 107401-79-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,0 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107401-79:
(8*1)+(7*0)+(6*7)+(5*4)+(4*0)+(3*1)+(2*7)+(1*9)=96
96 % 10 = 6
So 107401-79-6 is a valid CAS Registry Number.

107401-79-6Upstream product

107401-79-6Downstream Products

107401-79-6Relevant academic research and scientific papers

Studies on the Synthesis of 5-Acyl-2,4-diaminothiazoles from Amidinothioureas

Rajasekharan, K. N.,Nair, K. P.,Jenardanan, G. C.

, p. 353 - 355 (2007/10/02)

1-Alkyl or aryl-3-amidinothioureas with or without substituents on the amidino moiety react with α-haloketones to yield 5-acyl-2,4-diaminothiazoles.

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