3897-39-0

Basic information

• Product Name: N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE
• Synonyms: N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE;BUTTPARK 76\07-42
• CAS NO: 3897-39-0
• Molecular Formula: C₁₃H₁₃NO₃S
• Molecular Weight: 263.31
• Mol File: 3897-39-0.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 422°Cat760mmHg
• Flash Point: 209°C
• Appearance: /
• Density: 1.362g/cm³
• Vapor Pressure: 1.02E-07mmHg at 25°C
• Refractive Index: 1.645
• CAS DataBase Reference: N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE(3897-39-0)
• EPA Substance Registry System: N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE(3897-39-0)

Safety Data

• Hazardous Substances Data: 3897-39-0(Hazardous Substances Data)

Usage

General Description

N-(2-Hydroxy-phenyl)-4-methyl-benzenesulfonamide is a chemical compound with the molecular formula C13H13NO3S. It is a sulfonamide derivative and belongs to the class of organic compounds known as benzenesulfonamides. N-(2-HYDROXY-PHENYL)-4-METHYL-BENZENESULFONAMIDE is a white to off-white powder and is soluble in water, ethanol, and chloroform. It may have potential applications in pharmaceutical and medicinal fields due to its structural properties and potential interactions with biological targets. However, further research and testing are needed to determine its specific uses and effects.

InChI:InChI=1/C13H13NO3S/c1-10-6-8-11(9-7-10)18(16,17)14-12-4-2-3-5-13(12)15/h2-9,14-15H,1H3

Upstream product

• 623-11-0 1-methyl-4-nitrosobenzene 
• 95-55-6 2-amino-phenol 
• 98-59-9 p-toluenesulfonyl chloride 
• 1216-96-2 2-aminophenyl p-toluenesulfonate 
• 81256-20-4 2-{[(4-methylphenyl)sulfonyl]amino}phenyl 4-meythylbenzenesulfonate 
• 110-86-1 pyridine 
• 1624-49-3 2-(4-dimethylamino-benzylidenamino)-phenol 
• 107555-82-8 3-(p-tolylsulfonyl)-1,2,3-benzoxathiazole 2,2-dioxide 
• 129263-14-5 3a,4,5,7a-tetrahydrobenzo[d]oxazol-2(3H)-one 
• 941-55-9 4-toluenesulfonyl azide 
• 4783-68-0 2-phenoxypyridine 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 88-75-5 2-hydroxynitrobenzene 
• 65109-75-3 N-(phenoxy)-4-methylbenzenesulfonamide 

Downstream Products

• 169775-25-1 N-Tosylbenzophenoxazine-6,11-dione 
• 858842-60-1 toluene-4-sulfonic acid-(2-hydroxy-3,5-dinitro-anilide) 
• 53691-08-0 1-benzoyloxy-2-(toluene-4-sulfonylamino)-benzene 
• 81256-20-4 2-{[(4-methylphenyl)sulfonyl]amino}phenyl 4-meythylbenzenesulfonate 
• 70376-37-3 3-(p-tolylsulfonyl)-1,2,3-benzoxathiazole 2-oxide 
• 35970-37-7 ethyl 3,4-dihydro-4-tosyl-2H-1,4-benzoxazine-3-carboxylate 
• 109586-41-6 2-((4-methylbenzenesulfonyl)amino)phenyl trifluoromethanesulfonate 
• 107555-82-8 3-(p-tolylsulfonyl)-1,2,3-benzoxathiazole 2,2-dioxide 
• 86267-87-0 3,4-dihydro-4-tosyl-2H-1,4-benzoxazin-2-carbonitril 
• 70-55-3 toluene-4-sulfonamide 
• 473556-42-2 N-allyl-N-[2-(allyloxy)phenyl]-4-methylbenzenesulfonamide 
• 847198-44-1 3-oxo-2-thioxo-1-tosyl-2-phenoxy-4,5-benzo-1,2-azaphospholidine 
• 847198-47-4 {[2-oxo-3-(toluene-4-sulfonyl)-2,3-dihydro-2λ⁵-benzo[1,3,2]oxazaphosphol-2-yl]-phenyl-amino}-acetic acid methyl ester 

Relevant articles and documents

Expeditious formal synthesis of (±)-epibatidine using diastereoselective bromohydroxylation of aminocyclohexene derivatives

Bromination and bromohydroxylation of oxazolidinones derived from cyclohexadiene have been studied in order to synthetize (±)-epibatidine 18. Bromohydroxylation of compound 2 led to a polyfunctionalized halohydrin 11a which could be further cyclized to azabicyclo[2.2.1]heptan-2-one 16 already described as a precursor of epibatidine 18.

Hexafluoroisopropanol (HFIP)-prompted rearrangement of N-phenoxysulfonamides for the direct assembly of ortho-sulfonamide phenols: A combined experimental and computational study

ortho-Sulfonamide phenols represent a class of attractive structural motifs in medicinal and synthetic chemistry. Herein an efficient metal-free rearrangement reaction has been developed for the construction of ortho-sulfonamide phenols via HFIP-prompted

Pd(II)-Catalyzed Enantioselective Ring-Contraction for the Construction of 1,4-Benzoxazines

Enantioselective ring-contraction reactions have not been widely reported. We have developed an enantioselective ring contraction of 5,6-dihydro-2H-benzo[b][1,4]oxazocines, affording enantiomerically enriched 3,4-dihydro-2H-1,4-benzoxazine derivatives as