83412-75-3 Usage
General Description
(6-Chloropyridazin-3-yl)cyanamide is a chemical compound with the molecular formula C5H3ClN4. It is a cyanamide derivative with a chloropyridazinyl group attached to the cyanamide functional group. (6-Chloropyridazin-3-yl)cyanamide is used in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and ability to form a wide range of derivatives. Additionally, (6-Chloropyridazin-3-yl)cyanamide has been studied for its potential biological activities, including its antimicrobial and anticancer properties. Its unique molecular structure and reactivity make it an important building block in the development of new chemical compounds with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 83412-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,1 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83412-75:
(7*8)+(6*3)+(5*4)+(4*1)+(3*2)+(2*7)+(1*5)=123
123 % 10 = 3
So 83412-75-3 is a valid CAS Registry Number.
83412-75-3Relevant articles and documents
Reactions of N-Heteroarylformamide Oximes and N-Heteroarylacetamide Oximes with N,N-Dimethylformamide Dimethyl Acetal. Synthesis of 2-Methyl-s-triazoloazines and N-Methylcyanoaminoazines
Stanovnik, Branko,Stimac, Anton,Tisler, Miha,Vercek, Bojan
, p. 577 - 583 (2007/10/02)
N-Heteroarylformamide oximes 3 (R = H) were converted with N,N-dimethylformamide dimethyl acetal (DMFDMA) into N-heteroaryl-N-methylcyanoamino compounds 5, as the main products.In some instances N-heteroarylcyanoamino compounds 4, cyanoimino compounds 7, and some other products, such as 9 and 10 were also formed.On the other hand, N-heteroarylacetamide oximes 3 (R = CH3) were cyclized under the same reaction conditions into 2-methyl-s-triazoloazines (6).N-Heteroarylacetamide O-methyl oximes 11 and 12 were prepared from the corresponding acetamidines 2 (R = CH3) and O-methylhydroxylamine.
