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(6-Chloropyridazin-3-yl)cyanamide, with the molecular formula C5H3ClN4, is a cyanamide derivative featuring a chloropyridazinyl group attached to the cyanamide functional group. This chemical compound is recognized for its versatile reactivity and potential in forming a broad spectrum of derivatives, making it a valuable component in the synthesis of pharmaceuticals and agrochemicals. Its unique molecular structure and reactivity also contribute to its significance as a building block for developing new chemical compounds with possible therapeutic applications.

83412-75-3

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83412-75-3 Usage

Uses

Used in Pharmaceutical Synthesis:
(6-Chloropyridazin-3-yl)cyanamide is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique reactivity allows for the creation of a wide range of pharmaceutical compounds, contributing to the development of novel treatments for different health conditions.
Used in Agrochemical Synthesis:
In the agrochemical industry, (6-Chloropyridazin-3-yl)cyanamide is utilized as a vital component in the production of various agrochemicals. Its ability to form diverse derivatives makes it a valuable asset in the development of new products for agricultural applications, such as pesticides and fertilizers.
Used in Antimicrobial Applications:
(6-Chloropyridazin-3-yl)cyanamide has been studied for its potential antimicrobial properties, making it a candidate for use in the development of new antimicrobial agents. Its unique molecular structure and reactivity could lead to the creation of effective compounds to combat various microbial infections.
Used in Anticancer Applications:
(6-Chloropyridazin-3-yl)cyanamide has also been investigated for its potential anticancer properties. (6-Chloropyridazin-3-yl)cyanamide is used as a starting material in the development of new anticancer drugs, with the aim of discovering novel therapeutic options for the treatment of various types of cancer.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic outcomes of (6-Chloropyridazin-3-yl)cyanamide-based compounds, drug delivery systems are being developed. These systems, which may include organic and metallic nanoparticles, aim to improve the delivery and efficacy of the compound in targeted applications, such as cancer treatment.

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.

83412-75-3Downstream Products

83412-75-3Relevant academic research and scientific papers

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.

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