17742-68-6 Usage
Description
N-(2,6-dichloro-4-nitrophenyl)acetamide is a synthetic organic compound with the molecular formula C8H6Cl2N2O3. It is a derivative of acetamide, featuring a phenyl ring with two chlorine atoms and a nitro group attached. Known for its antimicrobial properties, this compound is utilized in pharmaceutical development and chemical research.
Uses
Used in Pharmaceutical Development:
N-(2,6-dichloro-4-nitrophenyl)acetamide is used as an antimicrobial agent for the development of antimicrobial agents. Its properties contribute to the creation of compounds that can effectively combat various types of microbes.
Used in Chemical Research:
In the field of chemical research, N-(2,6-dichloro-4-nitrophenyl)acetamide serves as a reagent. It aids in the synthesis of a variety of pharmaceutical compounds, supporting the advancement of chemical science and medicine.
Used in Synthesis of Pharmaceutical Compounds:
N-(2,6-dichloro-4-nitrophenyl)acetamide is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the creation of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 17742-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,4 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17742-68:
(7*1)+(6*7)+(5*7)+(4*4)+(3*2)+(2*6)+(1*8)=126
126 % 10 = 6
So 17742-68-6 is a valid CAS Registry Number.
17742-68-6Relevant articles and documents
Activator free, expeditious and eco-friendly chlorination of activated arenes by N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI)
Misal, Balu,Palav, Amey,Ganwir, Prerna,Chaturbhuj, Ganesh
supporting information, (2021/01/04)
N-Chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI) has been explored for the first time as a chlorinating reagent for direct chlorination of various activated arenes and heterocycles without any activator. A comparative in-silico study was performed to determine the electrophilic character for NCBSI and commercially available N-chloro reagents to reveal the reactivity on a theoretical viewpoint. The reagent was prepared by an improved method avoiding the use of hazardous t-butyl hypochlorite. This reagent was proved to be very reactive compared to other N-chloro reagents. The precursor of the reagent N-(phenylsulfonyl)benzene sulfonamide was recovered from aqueous spent, which can be recycled to synthesize NCBSI. The eco-friendly protocol was equally applicable for the synthesis of industrially important chloroxylenol as an antibacterial agent.
