463-52-5 Usage
Uses
Used in Pharmaceutical Industry:
Formamidine is used as a pharmaceutical compound for its various applications in the medical field. It is known for its antimicrobial properties, making it effective against a range of bacteria, fungi, and protozoa. This characteristic allows formamidine to be utilized in the development of medications and treatments for various infections.
Used in Cosmetic Industry:
In the cosmetic industry, formamidine is used as a preservative due to its ability to inhibit the growth of microorganisms. This helps maintain the stability and shelf life of cosmetic products, ensuring their safety and efficacy for consumers.
Used in Agricultural Industry:
Formamidine is also employed in the agricultural sector as a pesticide, particularly for the control of various pests and diseases affecting crops. Its antimicrobial properties contribute to the protection of plants from harmful microorganisms, thereby enhancing crop yield and quality.
Used in Research and Development:
In the field of research and development, formamidine serves as a valuable compound for studying the properties and behavior of carboxamidines. Its unique structure and functional groups make it an interesting subject for chemical and biological investigations, potentially leading to the discovery of new applications and uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 463-52-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 463-52:
(5*4)+(4*6)+(3*3)+(2*5)+(1*2)=65
65 % 10 = 5
So 463-52-5 is a valid CAS Registry Number.
463-52-5Relevant articles and documents
Iodine Catalyzed Oxidative Coupling of Diaminoazines and Amines for the Synthesis of 3,5-Disubstituted-1,2,4-Triazoles
Beifuss, Uwe,Bharatam, Prasad V.,Chourasiya, Sumit S.,Kathuria, Deepika,Sahoo, Subash C.,Wani, Aabid A.
, p. 7659 - 7671 (2021/06/25)
A simple, convenient, transition metal-free one pot synthesis of 3,5-disubstituted-1,2,4-triazoles has been established. The innovation in this reaction is the use of easily available 1,1-diaminoazines as substrates. This method provides the products with wider substrate scope, at an expedited rate, and with relatively better yields in comparison to the reported methods. The reaction mechanism involves an initial intermolecular nucleophilic addition (facilitated by I2) followed by intramolecular nucleophilic cyclization.