74840-99-6 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals. Its antimicrobial properties make it a key component in the development of medications targeting fungal and bacterial infections.
Used in Agrochemical Industry:
In the agrochemical industry, Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate is utilized as an intermediate for the synthesis of compounds that help protect crops from microbial infections, thereby ensuring higher crop yields and quality.
Used in Organic Compounds Synthesis:
Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate is also used as an intermediate in the synthesis of other organic compounds, contributing to the creation of a wide range of products across different industries.
It is important to handle Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate with care, as it is toxic if ingested and may cause irritation to the skin and eyes upon contact. Despite these precautions, Ethyl 4,5-dibromo-1H-imidazole-2-carboxylate plays a vital role in the development of various therapeutic and agricultural products, underscoring its importance in modern chemistry and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 74840-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74840-99:
(7*7)+(6*4)+(5*8)+(4*4)+(3*0)+(2*9)+(1*9)=156
156 % 10 = 6
So 74840-99-6 is a valid CAS Registry Number.
74840-99-6Relevant academic research and scientific papers
Syntheses and Reactions of Some 4,5-Dihaloimidazole-2-carboxylic Acid Derivatives
Dirlam, John P.,James, Richard B.,Shoop, Eleanor V.
, p. 409 - 411 (2007/10/02)
The preparation of 5H,10H-diimidazopyrazine-5,10-dione (2a) and its 2,3,7,8-tetrabromo- and 2,3,7,8-tetrachloro- analogs (2b and 2c, respectively) is reported.These dimers, when allowed to react with various anilines, afford imidazole-2-carboxamides (3a-c).
