856856-72-9 Usage
Sulfonylurea compound
Commonly used in synthesis of pharmaceutical drugs and agrochemicals
As a sulfonylurea compound, it is widely utilized in the production of various pharmaceutical and agrochemical products due to its versatile chemical properties.
Derivative of acetamide
With a toluene-4-sulfonylimino group attached to the 2H-pyridin-1-yl moiety
2-[2-(Toluene-4-sulfonyliMino)-2H-pyridin-1-yl]-acetaMide is derived from acetamide by attaching a toluene-4-sulfonylimino group to the 2H-pyridin-1-yl moiety, which contributes to its unique chemical properties and potential applications.
Potential biological activities
Antifungal and antibacterial properties
2-[2-(Toluene-4-sulfonylimino)-2H-pyridin-1-yl]-acetamide has been studied for its potential biological activities, including its ability to exhibit antifungal and antibacterial properties, making it a potential candidate for the development of new drugs.
Building block for synthesis
Various organic compounds in medicinal and agricultural chemistry
2-[2-(Toluene-4-sulfonyliMino)-2H-pyridin-1-yl]-acetaMide serves as a building block for the synthesis of a wide range of organic compounds, which can be used in the development of new pharmaceutical and agrochemical products.
Importance in industries
Pharmaceutical and agrochemical applications
Due to its unique properties and potential applications, 2-[2-(Toluene-4-sulfonylimino)-2H-pyridin-1-yl]-acetamide is considered an important chemical intermediate in the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 856856-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,8,5 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 856856-72:
(8*8)+(7*5)+(6*6)+(5*8)+(4*5)+(3*6)+(2*7)+(1*2)=229
229 % 10 = 9
So 856856-72-9 is a valid CAS Registry Number.
856856-72-9Relevant academic research and scientific papers
Selective C-acylation of 2-aminoimidazo[1,2- a ]pyridine: Application to the synthesis of imidazopyridine-fused [1,3]diazepinones
Masurier, Nicolas,Aruta, Roberta,Gaumet, Vincent,Denoyelle, Severine,Moreau, Emmanuel,Lisowski, Vincent,Martinez, Jean,Maillard, Ludovic T.
experimental part, p. 3679 - 3685 (2012/05/20)
A series of 20 optically pure 3,4-dihydro-5H-pyrido[1′,2′:1,2] imidazo[4,5-d][1,3]diazepin-5-ones which form a new family of azaheterocycle-fused [1,3]diazepines were synthesized in four steps with 17-66% overall yields. The key step consists of a selecti
