83209-82-9

Basic information

• Product Name: N-[2-METHOXY-4-(METHYLSULFONYLAMINO)PHENYL]ACETAMIDE
• Synonyms: N-[2-METHOXY-4-(METHYLSULFONYLAMINO)PHENYL]ACETAMIDE
• CAS NO: 83209-82-9
• Molecular Formula: C₁₀H₁₄N₂O₄S
• Molecular Weight: 258.29
• Mol File: 83209-82-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[2-METHOXY-4-(METHYLSULFONYLAMINO)PHENYL]ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-METHOXY-4-(METHYLSULFONYLAMINO)PHENYL]ACETAMIDE(83209-82-9)
• EPA Substance Registry System: N-[2-METHOXY-4-(METHYLSULFONYLAMINO)PHENYL]ACETAMIDE(83209-82-9)

Safety Data

• Hazardous Substances Data: 83209-82-9(Hazardous Substances Data)

Upstream product

• 93-27-6 5-nitro-2-acetylaminoanisole 
• 124-63-0 methanesulfonyl chloride 
• 97-52-9 2-methoxy-4-nitrophenylamine 
• 5329-15-7 N-(4-amino-2-methoxyphenyl)acetamide 

Downstream Products

• 106994-16-5 2-{[4-(Allyl-methanesulfonyl-amino)-2-methoxy-5-nitro-phenyl]-hydrazono}-butyric acid ethyl ester 
• 92138-16-4 9-(4-Methanesulfonylamino-2-methoxy-phenylamino)-5-methyl-acridine-4-carboxylic acid methylamide; hydrochloride 
• 116911-57-0 2-[4-(Allyl-methanesulfonyl-amino)-2-methoxy-5-nitro-phenylazo]-2-ethyl-3-oxo-butyric acid ethyl ester 
• 106994-16-5 2-methoxy-5-nitro-4-phenylhydrazone of ethyl 2-oxobutenoate 
• 116911-56-9 N-(4-acetamido-5-methoxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide 
• 106994-15-4 N-(4-amino-5-methoxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide 
• 57165-06-7 N-(4-amino-3-methoxyphenyl)methanesulfonamide 
• 116911-55-8 N-(4-acetamido-5-mthoxy-2-nitrophenyl)methanesulfonamide 

Relevant articles and documents

Anticancer anilinoacridines. A process synthesis of the disubstituted amsacrine analog CI-921

An improved process for the synthesis of bulk quantities of the clinical amsacrine analog CI-921 is reported. Described also are detailed analytical and spectroscopic data for this agent.

PHOTOCHEMISTRY OF QUINONE DIAZIDES. INTRAMOLECULAR OXYGEN TRANSFER AND CARBENOID ADDITION DURING PHOTOLYSIS OF N-ALLYLSULFONAMIDO QUINONE DIAZIDES

An indole quinone diazide, 5-(N-allylsulfonamido)-4-diazo-3-methyl-4,7-dihydroindol-7-one, which is a potential precursor of a spiro-cyclopropane-indol-7-one structure has been prepared.A study of its photolysis and that of a model compound has identified oxygen transfer from the sulfonamido substituent as a process which competes with intramolecular carbenoid addition.