16678-85-6 Usage
Uses
Used in Pharmaceutical Industry:
Benzamide, N-sulfonylis utilized as a reagent in the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic benefits, contributing to the development of novel treatments for a range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, Benzamide, N-sulfonylserves as a key component in the production of various agrochemicals. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases, thereby supporting agricultural productivity and food security.
Used in Materials Science:
Benzamide, N-sulfonylis also applied in the field of materials science, where it contributes to the development of new materials with specific properties. Its versatility in chemical reactions allows for the creation of materials with tailored characteristics for use in various applications, such as coatings, adhesives, or advanced composites.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, Benzamide, N-sulfonylis employed as an antimicrobial agent in various settings. It can be incorporated into products to prevent the growth of harmful microorganisms, thereby reducing the risk of infections and maintaining cleanliness and hygiene.
Used in Analgesic and Anti-inflammatory Applications:
Benzamide, N-sulfonylalso exhibits analgesic and anti-inflammatory properties, making it a potential candidate for the development of pain relief and anti-inflammatory medications. Its incorporation into pharmaceutical formulations could provide effective treatments for conditions characterized by pain and inflammation.
Check Digit Verification of cas no
The CAS Registry Mumber 16678-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16678-85:
(7*1)+(6*6)+(5*6)+(4*7)+(3*8)+(2*8)+(1*5)=146
146 % 10 = 6
So 16678-85-6 is a valid CAS Registry Number.
16678-85-6Relevant academic research and scientific papers
Tornus, Ingo,Schaumann, Ernst,Adiwidjaja, Gunadi
, p. 1629 - 1633 (1996)
Reaction of 3-dimethylamino-2,2-diphenyl-2H-azirine 3a with N-sulfonylalkylamines 2a,b provides 1,2,5-thiadiazoles 5a,b, whereas use of N-carbonylsulfonylamines 2c,e as reaction partners primarily results in 1,2,3-oxathiazoles 6a,b which isomerise to the corresponding thiadiazoles 5c,d on treatment with silica gel at room temperature. In contrast, use of 2-alkyl-3-dimethylamino-2-phenyl-2H-azirines 3b,c in the reaction with the N-sulfonylamide 2c and the N-sulfonylcarbamates 2e,f leads to mixtures of thiadiazoles 5 and oxathiazoles 6 along with isomeric acrylamidines 7.
The Introduction of Nitrile-Groups into Heterocycles and Concversion of Carboxylic Groups into their Corresponding Nitriles with Clorosulfonylisocyanate and Triethylamine
Vorbrueggen, Helmut,Krolikiewicz, Konrad
, p. 6549 - 6558 (2007/10/02)
Addition of chlorosulfonylisocyanate (CSI) to heterocycles such as thiophene (4) or indole (15) and unsaturated systems such as dihydropyran (7) gives N-chlorosulfonylamides RCONHSO2Cl, which can be converted by equivalent amounts of triethylamine to their corresponding nitriles.Since carboxylic acids react with CSI to N-chlorosulfonylamides, subsequent treatment with triethylamine affords the corresponding nitriles, but no isocyanates as claimed by other authors.The mechanisms of the conversion of the intermediate N-chlorosulfonylamides into the corresponding nitriles are discussed.
