141563-06-6 Usage
General Description
1,5-DIAMINO-4-CYANOIMIDAZOLE is a chemical compound that consists of two amino groups and a cyano group attached to a 4,5-dihydroimidazole ring structure. It is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds and as an intermediate in the production of dyes and pigments. Its versatile properties also make it suitable for use in organic synthesis, coordination chemistry, and catalysis. Additionally, 1,5-DIAMINO-4-CYANOIMIDAZOLE has potential applications in materials science, particularly in the development of new polymers and coatings due to its unique chemical structure and reactivity. Overall, the compound has a wide range of industrial and research applications, making it an important chemical in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 141563-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,6 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141563-06:
(8*1)+(7*4)+(6*1)+(5*5)+(4*6)+(3*3)+(2*0)+(1*6)=106
106 % 10 = 6
So 141563-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H5N5/c5-1-3-4(6)9(7)2-8-3/h2H,6-7H2
141563-06-6Relevant articles and documents
(Z)-N3-(2-Amino-1,2-dicyanovinyl)formamidrazone: a Precursor in the Synthesis of 1,5-Diaminoimidazoles and 6-Carbamoyl-1,2-dihydropurines
Alves, M. Jose,Booth, Brian L.,Freitas, A. Paula,Proenca, M. Fernanda J. R. P.
, p. 913 - 917 (2007/10/02)
The reaction of ethyl (Z)-N-(2-amino-1,2-dicyanovinyl)formimidate with hydrazine monohydrate leads to (Z)-N3-(2-amino-1,2-dicyanovinyl)formamidrazone in almost quantitative yield.This compound proved to be an important starting material for the synthesis of the corresponding N1-isopropylidene- and N1-acetyl-formamidrazones.The amidrazones prepared promptly cyclize in the presence of base to give a 1,5-diamino-4-cyanoimidazole or a 1,5-diamino-4-(cyanoformimidoyl)imidazole, depending on the reaction conditions and mainly on the nature of the base used to induce cyclization. 1,5-Diamino-4-(cyanoformimidoyl)imidazole was treated with carbonyl compounds and the 1,2-dihydropurines thus isolated indicated that the amino group in position 5 is more reactive than that in position 1.
