5539-46-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
5-aminothiazole-4-carboxamide is utilized as a key intermediate in the synthesis of antitumor and antifungal agents, contributing to the development of new drugs with enhanced therapeutic properties.
Used in the Synthesis of Pharmaceuticals:
5-aminothiazole-4-carboxamide serves as a precursor in the production of various pharmaceuticals, leveraging its chemical reactivity and structural features to create a wide range of therapeutic compounds.
Used in the Synthesis of Agrochemicals:
In the agrochemical industry, 5-aminothiazole-4-carboxamide is employed as a building block for the development of new agrochemicals, potentially leading to more effective and targeted pest control solutions.
Used in the Synthesis of Fine Chemicals:
5-aminothiazole-4-carboxamide is also used in the synthesis of fine chemicals, where its unique structure and properties can be harnessed to create specialty compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5539-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5539-46:
(6*5)+(5*5)+(4*3)+(3*9)+(2*4)+(1*6)=108
108 % 10 = 8
So 5539-46-8 is a valid CAS Registry Number.
5539-46-8Relevant academic research and scientific papers
Short and efficient synthesis of 5-aminothiazole-4-carboxamide
Wang, Jin,Guo, Jianyu,Tang, Yihong,Zhang, Suxia,Tao, Jianwei,Lu, Yan
, p. 175 - 176 (2014/07/07)
5-Aminothiazole-4-carboxamide is a precursor for the synthesis of thiazole [4,5-d] pyrimidines. In this work, a new synthesis method with a high total yield (79%) of 5-aminothiazole-4-carboxamide was reported. The starting material is aminocyanacetamide. This synthesis method is environment-friendly and is suitable for industrial production.
Novel analogues of tiazofurin by Lawesson reagent effected cyclization
Golankiewicz,Januszczyk
, p. 313 - 316 (2007/10/02)
2-Benzylthiazole-4-carboxamide 4 and 5-(β-D-ribofuranosylamino) thiazole-4-carboxamide 10 were synthesized from phenylacetylamino- and formylamino cyanoacetic acid esters 1a and 1b, respectively. The ribosylation reaction leading to 10 gave rise also to i
