15020-57-2

Basic information

• Product Name: P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE
• Synonyms: P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE;4-Hydroxy-N,N-dimethylbenzenesulfonamide;N,N-Dimethyl-4-hydroxybenzenesulfonamide;N,N-dimethyl-4-hydroxybenzenesulphonamide
• CAS NO: 15020-57-2
• Molecular Formula: C₈H₁₁NO₃S
• Molecular Weight: 201.24
• Mol File: 15020-57-2.mol
• Article Data: 7

Chemical Properties

• Melting Point: 95 °C
• Boiling Point: 347.3°Cat760mmHg
• Flash Point: 163.9°C
• Appearance: /
• Density: 1.3156 (rough estimate)
• Vapor Pressure: 2.7E-05mmHg at 25°C
• Refractive Index: 1.5364 (estimate)
• PKA: 7.81±0.13(Predicted)
• CAS DataBase Reference: P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE(15020-57-2)
• EPA Substance Registry System: P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE(15020-57-2)

Safety Data

• Hazardous Substances Data: 15020-57-2(Hazardous Substances Data)

Usage

Uses

4-Dimethylsulfamoylphenol is a useful synthetic intermediate. 4-Dimethylsulfamoylphenol can be used as a reagent to synthesize N-(4-ethoxyphenyl)-4-[hydroxy(diphenyl)methyl]piperidine-1-carbothioamide derivs. as neuropeptide Y Y2 receptor antagonists.

InChI:InChI=1/C8H11NO3S/c1-9(2)13(11,12)8-5-3-7(10)4-6-8/h3-6,10H,1-2H3

Upstream product

• 66950-63-8 phenyl N,N-dimethylsulfamate 
• 79119-26-9 4-acetoxybenzenesulfonyl chloride 
• 506-59-2 N,N-dimethylammonium chloride 
• 383-31-3 4-fluoro-1-(N,N-dimethylaminosulfonyl)benzene 
• 59907-37-8 N,N-dimethyl-4-methoxybenzenesulfonamide 
• 825-90-1 sodium p-hydroxybenzenesulfonate 
• 4025-67-6 4-hydroxybenzene-1-sulfonyl chloride 
• 124-40-3 dimethyl amine 
• 368-87-6 4-hydroxybenzene-1-sulfonyl fluoride 
• 7463-22-1 N,N-Dimethyl-p-chlorobenzenesulfonamide 

Downstream Products

• 41989-56-4 Isopropoxymethyl-phosphonothioic acid O-(4-dimethylsulfamoyl-phenyl) ester O-ethyl ester 
• 1383479-24-0 C₂₇H₃₀N₂O₅S 
• 32547-91-4 N,N-dimethyl-4-(prop-2-ynyloxy)benzenesulfonamide 
• 61712-33-2 2,6-Dibromo-N,N-dimethyl-1-phenol-4-sulfonamide, propionate 
• 1196485-25-2 4-[4-(4-dimethylsulfamoyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester 
• 30989-03-8 2-chloro-N,N-dimethyl-1-phenol-4-sulfonamide 
• 61712-32-1 2,6-dichloro-N,N-dimethyl-1-phenol-4-sulfonamide 
• 31972-17-5 2,6-dibromo-N,N-dimethyl-1-phenol-4-sulfonamide 
• 76472-25-8 p-(p-Guanidinobenzoyloxy)-N,N-dimethylbenzenesulfonamide methanesulfonic acid salt 
• 100245-27-0 1-(4-Methoxy-benzyl)-1H-tetrazole-5-carboxylic acid (5-dimethylsulfamoyl-2-hydroxy-phenyl)-amide 
• 100245-58-7 1H-Tetrazole-5-carboxylic acid (5-dimethylsulfamoyl-2-hydroxy-phenyl)-amide 
• 24962-75-2 3-amino-4-hydroxy-N,N-dimethylbenzenesulphonamide 
• 42247-91-6 4-hydroxy-N,N-dimethyl-3-nitrobenzenesulfonamide 
• 51005-99-3 Methoxymethyl-phosphonic acid 4-dimethylsulfamoyl-phenyl ester ethyl ester 

Relevant articles and documents

A new synthetic route to aryl hydroxysulfonamides via a novel Fries-type rearrangement of aryl N,N-dialkylsulfamates

A novel thia-Fries rearrangement of sulfamates 1 in AlCl3 giving good yields of para-2 and ortho-3 arylhydroxysulfonamides offers a new and efficient route to these sulfonamides.

INDOLE AND AZAINDOLE HALOALLYLAMINE DERIVATIVE INHIBITORS OF LYSYL OXIDASES AND USES THEREOF

The present invention relates to novel compounds which are capable of inhibiting certain amine oxidase enzymes. These compounds are useful for treatment of a variety of indications, e.g., fibrosis, cancer and/or angiogenesis in human subjects as well as i

MORPHOLINYL SUBSTITUTED [1,2,4]-TRIAZOLO[1,5-A]TRIAZINE AS ANTAGONIST

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