570407-10-2 Usage
Description
2-Thiazolamine, 4-(4-chloro-2-thienyl)is an organic compound that features a thiazolamine core with a 4-chloro-2-thienyl substituent. This unique molecular structure endows it with potential applications in various fields, particularly in organic synthesis and pharmaceutical chemistry.
Uses
Used in Organic Synthesis:
2-Thiazolamine, 4-(4-chloro-2-thienyl)is used as an organic synthesis intermediate for the preparation of various complex organic molecules. Its unique structure allows for the formation of diverse chemical entities, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Thiazolamine, 4-(4-chloro-2-thienyl)is utilized as a pharmaceutical intermediate. Its incorporation into drug molecules can potentially lead to the development of new therapeutic agents with novel mechanisms of action. 2-Thiazolamine, 4-(4-chloro-2-thienyl)-'s reactivity and structural features make it a promising candidate for the design and synthesis of innovative pharmaceuticals.
Used in Laboratory Research and Development:
2-Thiazolamine, 4-(4-chloro-2-thienyl)is also employed in laboratory research and development processes. Researchers use this compound to explore its chemical properties, reactivity, and potential applications in various chemical reactions. Its use in research settings aids in the advancement of knowledge in organic and medicinal chemistry.
Used in Chemical Production Processes:
Furthermore, 2-Thiazolamine, 4-(4-chloro-2-thienyl)is used in chemical production processes, where it serves as a key intermediate in the synthesis of various chemical products. Its role in these processes is crucial for the efficient and scalable production of target molecules, contributing to the overall chemical industry's growth and innovation.
Synthesis
Bromine was added to an ether solution of 4-chloro-2-acetylthiophene under ice cooling, and the mixture was stirred at room temperature for 2 hours to obtain a brominated compound. Thiourea was added to an EtOH solution of the brominated compound at room temperature, and the mixture was stirred overnight at 80°C to obtain 2-amino-4-(4-chlorothiophen-2-yl)thiazole.
Check Digit Verification of cas no
The CAS Registry Mumber 570407-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,0,4,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 570407-10:
(8*5)+(7*7)+(6*0)+(5*4)+(4*0)+(3*7)+(2*1)+(1*0)=132
132 % 10 = 2
So 570407-10-2 is a valid CAS Registry Number.
570407-10-2Relevant articles and documents
Synthesis and Antibacterial Activity of Benzazolyl Azolyl Sulfamoyl Acetamides
Rajeswari, Tankam,Rekha, Tamatam,Dinneswara Reddy, Guda,Padmaja, Adivireddy,Padmavathi, Venkatapuram
, p. 2449 - 2459 (2019/08/07)
A new class of benzazolyl azolyl sulfamoyl acetamides was prepared from azolyl sulfamoyl acetates and benzazolyl amines in the presence of KOtBu in tetrahydrofuran. Compounds with benzothiazole-thiazole, benzimidazole-thiazole, benzothiazole-imidazole, and benzimidazole-imidazole moieties exhibited excellent antibacterial activity against Bacillus subtilis.
2-ACYLAMINOTHIAZOLE DERIVATIVE OR SALT THEREOF
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Page 16, (2010/02/08)
A 2-acylaminothiazole derivative or a pharmaceutically acceptable salt thereof having an excellent effect of proliferating human c-mpl-Ba/F3 cells and an activity of increasing platelets based on the effect of promoting the formation of megakaryocytic colonies. A compound or a pharmaceutically acceptable salt thereof useful in treating thrombocytopenia.
