27332-20-3

Basic information

• Product Name: 2-AMINO-N-PHENYL-BENZENESULFONAMIDE
• Synonyms: BenzenesulfonaMide, 2-aMino-N-phenyl-
• CAS NO: 27332-20-3
• Molecular Formula: C₁₂H₁₂N₂O₂S
• Molecular Weight: 248.3009
• Mol File: 27332-20-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 439.8°Cat760mmHg
• Flash Point: 219.8°C
• Appearance: /
• Density: 1.373g/cm³
• Vapor Pressure: 6.19E-08mmHg at 25°C
• Refractive Index: 1.669
• CAS DataBase Reference: 2-AMINO-N-PHENYL-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-N-PHENYL-BENZENESULFONAMIDE(27332-20-3)
• EPA Substance Registry System: 2-AMINO-N-PHENYL-BENZENESULFONAMIDE(27332-20-3)

Safety Data

• Hazardous Substances Data: 27332-20-3(Hazardous Substances Data)

Usage

General Description

2-Amino-N-phenyl-benzenesulfonamide is a chemical compound that is also known as N-phenyl-2-aminobenzenesulfonamide. It is represented by the molecular formula C12H12N2O2S. 2-AMINO-N-PHENYL-BENZENESULFONAMIDE is used in various industrial applications, and carries substantial relevance in organic chemistry. Structurally, it encompasses functional groups like sulfonamide, aromatic amine, and arylamine. It is critical to handle this compound with care due to possible risks and hazards associated with it. The material safety data sheets (MSDS) should be referred for detailed safety information.

InChI:InChI=1/C12H12N2O2S/c13-11-8-4-5-9-12(11)17(15,16)14-10-6-2-1-3-7-10/h1-9,14H,13H2

Upstream product

• 4837-33-6 o-nitrobenzenesulfenanilide 
• 5454-97-7 2-nitro-N-phenylbenzenesulfonamide 
• 23773-60-6 2-phenyl-2H-1,2,4-benzothiadiazine 1,1-dioxide 
• 101954-71-6 N-(2'-formamidobenzenesulfonyl)aniline 
• 587-14-4 N,N'-diphenylsulfamide 
• 62-53-3 aniline 
• 4837-32-5 S-(2-nitrophenyl)-N-(p-tolyl)thiohydroxylamine 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 

Downstream Products

• 18127-45-2 2-phenyl-2H-benzo[e][1,2,3,4]thiatriazine-1,1-dioxide 
• 110194-85-9 3-oxo-3-phenyl-propionic acid-(2-phenylsulfamoyl-anilide) 
• 23773-60-6 2-phenyl-2H-1,2,4-benzothiadiazine 1,1-dioxide 
• 101954-71-6 N-(2'-formamidobenzenesulfonyl)aniline 
• 101954-59-0 3-methyl-2-phenyl-2H-1,2,4-benzothiadiazine 1,1,-dioxide 
• 91823-26-6 2-phenyl-3-thioxo-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide 
• 1864-33-1 9,9-dioxo-10H-9-thia-10-aza-phenanthrene 
• 885683-53-4 C₁₈H₁₅N₃O₆S₂ 
• 885683-54-5 C₁₈H₁₇N₃O₄S₂ 
• 53347-49-2 2,2'-diaminodiphenyl sulfone 
• 88312-86-1 6-phenyl-6H-dibenzo<1,2>thiazin 5,5-dioxide 
• 120831-28-9 2-(4-diethylamino-2-methyl-phenylimino)-3-oxo-3-phenyl-propionic acid-(2-phenylsulfamoyl-anilide) 
• 203932-91-6 2-azido-N-phenylbenzenesulfonamide 

Relevant articles and documents

Palladium(0)-catalysed regioselective cyclisations of 2-amino(tosyl) benzamides/sulphonamides: The stereoselective synthesis of 3-ylidene-[1,4]benzodiazepin-5-ones/benzo[f][1,2,5]thiadiazepine-1,1-dioxides

The Pd(0) catalysed cyclisation reactions betweentert-butyl propargyl carbonates and 2-aminotosyl benzamides or sulphonamides deliver 1,4-benzodiazepin-5-ones or sultam derivatives, key components of many biologically active compounds. But 2-amino benzamides/sulphonamides require propargyl carbonates substituted at acetylenic carbon to undergo the reaction resulting in the stereoselective formation of the said products.

Transition-Metal-Free Tandem Cyclization/ N-Arylation Reaction: A Method to Access Biaryl Sultam Derivatives via a Diradical Pathway

A novel procedure for the transition-metal-free tandem cyclization/N-arylation reaction sequence of an aryne with a 1,2,3,4-benzothiatriazine-1,1-dioxide is reported. This reaction goes through the intramolecular homolytic cyclization to generate an N-H b

Dibenzo[1,2,5]thiadiazepines are non-competitive GABAA receptor antagonists

A new process for obtaining dibenzo[c,f][1,2,5]thiadiazepines (DBTDs) and their effects on GABAA receptors of guinea pig myenteric neurons are described. Synthesis of DBTD derivatives began with two commercial aromatic compounds. An azide group was obtain