74875-17-5 Usage
Uses
Used in Organic Synthesis:
2,6-dichloro-4-nitrobenzenesulfonyl chloride is utilized as a reagent in organic synthesis for the preparation of a variety of sulfonamides and sulfones. Its high electrophilicity makes it a valuable component in creating new organic compounds with specific properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,6-dichloro-4-nitrobenzenesulfonyl chloride is employed as a modifying agent to alter the properties of organic molecules, enabling the development of new compounds with targeted therapeutic effects.
Used in Agrochemical Production:
Similarly, in agrochemicals, 2,6-dichloro-4-nitrobenzenesulfonyl chloride is used to modify existing molecules, leading to the creation of new compounds with specific pesticidal or herbicidal properties, thereby enhancing crop protection strategies.
Safety Considerations:
It is crucial to handle 2,6-dichloro-4-nitrobenzenesulfonyl chloride with care due to its corrosive nature, which can result in skin, eye, and respiratory irritation. Proper safety measures should be implemented during its use to mitigate potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 74875-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,7 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74875-17:
(7*7)+(6*4)+(5*8)+(4*7)+(3*5)+(2*1)+(1*7)=165
165 % 10 = 5
So 74875-17-5 is a valid CAS Registry Number.
74875-17-5Relevant academic research and scientific papers
Anticoccidial derivatives of 6-azauracil. 3. Synthesis, high activity, and short plasma half-life of 1-phenyl-6-azauracils containing sulfonamide substituents
Miller,Mylari,Howes Jr.,Figdor,Lynch,Lynch,Koch
, p. 1083 - 1087 (2007/10/02)
A series of 1-phenyl-6-azauracils containing sulfonamide substituents was prepared. In contrast to previous 1-phenyl-6-azauracils, some of these sulfonamides combine high activity against Eimeria tenella infections in chickens with a very rapid rate of clearance from plasma. Most active was 1-[3'-chloro-5'-methyl-4'-(morpholinyl-sulfonyl)phenyl]-6-azauracil, with a minimum effective concentration in feed of about 10 ppm.
