6590-65-4

Basic information

• Product Name: N-(2-FORMYLPHENYL)-4-METHYL-BENZENESULF&
• Synonyms: N-(2-FORMYLPHENYL)-4-METHYL-BENZENESULF&
• CAS NO: 6590-65-4
• Molecular Formula: C₁₄H₁₃NO₃S
• Molecular Weight: 275.327
• Mol File: 6590-65-4.mol
• Article Data: 75

Chemical Properties

• Melting Point: 203-205 °C
• Boiling Point: 445.1°C at 760 mmHg
• Flash Point: 223°C
• Appearance: /
• Density: 1.333g/cm³
• Vapor Pressure: 4.05E-08mmHg at 25°C
• Refractive Index: 1.63
• PKA: 7.94±0.10(Predicted)
• CAS DataBase Reference: N-(2-FORMYLPHENYL)-4-METHYL-BENZENESULF&(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-FORMYLPHENYL)-4-METHYL-BENZENESULF&(6590-65-4)
• EPA Substance Registry System: N-(2-FORMYLPHENYL)-4-METHYL-BENZENESULF&(6590-65-4)

Safety Data

• Hazardous Substances Data: 6590-65-4(Hazardous Substances Data)

Usage

General Description

N-(2-Formylphenyl)-4-methyl-benzenesulfonamide is a chemical compound with the molecular formula C14H13NO2S. It is a sulfonamide derivative, which is a class of organic compounds that contain a sulfonyl functional group attached to an amino group. This specific compound is characterized by a benzene ring with a formyl group at the 2-position and a methyl group at the 4-position. Sulfonamides are commonly used as antimicrobial agents and in the synthesis of pharmaceutical drugs. The compound's properties and potential applications are further determined through research and testing in various chemical and biological studies.

InChI:InChI=1/C14H13NO3S/c1-11-6-8-13(9-7-11)19(17,18)15-14-5-3-2-4-12(14)10-16/h2-10,15H,1H3

Upstream product

• 529-23-7 o-aminobenzaldehyde 
• 98-59-9 p-toluenesulfonyl chloride 
• 89-98-5 2-chloro-benzaldehyde 
• 70-55-3 toluene-4-sulfonamide 
• 941-55-9 4-toluenesulfonyl azide 
• 5908-41-8 benzoyltrimethylsilane 
• 271-58-9 anthranil 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 5344-90-1 2-Aminobenzyl alcohol 
• 612-25-9 2-Nitrobenzyl alcohol 
• 552-89-6 2-nitro-benzaldehyde 
• 197847-57-7 N-[2-(hydroxymethyl)phenyl]benzenesulfonamide 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 100-52-7 benzaldehyde 

Downstream Products

• 136117-42-5 N-(o-tosylaminobenzylidene)ethylamine 
• 182145-40-0 N-[2-(1-Hydroxyhept-6-enyl)phenyl]-4-methylbenzenesulfonamide 
• 705256-10-6 N-[2-(benzyloxyimino-methyl)-phenyl]-4-methyl-benzenesulfonamide 
• 130725-49-4 bis{N-[2-[(Z)-3-hydroxypropyliminomethyl]phenyl]-4-methylbenzenesulfonamide}zinc(II) 
• 1236231-21-2 CH₃C₆H₄SO₂NHC₆H₄CHN(C₇H₁₅) 
• 134071-62-8 CH₃C₆H₄SO₂NHC₆H₄CHN(C₁₈H₃₇) 
• 1244956-21-5 4-(2'-tosylaminobenzylidene)amino-1,2,4-triazoline-5-thione 
• 1244956-22-6 3-methyl-4-(2'-tosylaminobenzylidene)amino-1,2,4-triazoline-5-thione 
• 1393131-07-1 N-(2-((E)-3-oxo-3-phenylprop-1-en-1-yl)phenyl)-N-tosylbenzamide 
• 1393131-24-2 (Z)-1-phenyl-2-(2-phenyl-1-tosyl-1H-indol-3-yl)vinyl benzoate 
• 1195694-52-0 4-methyl-N-(2-((E)-3-oxo-3-phenylprop-1-en-1-yl)phenyl)benzenesulfonamide 
• 1448808-99-8 2-(iodomethylene)-1-tosylindolin-3-one 
• 228720-21-6 [Cu₂(N(SO₂C₆H₄CH₃)C₆H₄CHNC₆H₄O)2] 
• 134424-69-4 (C₆H₄(CHNC₆H₄NO₂)(NSO₂C₆H₄CH₃))2Zn 

Relevant articles and documents

Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: Synthesis of trans-2,3-disubstitued indolines

Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates has been achieved, giving trans-2,3-disubstitued indolines as major diastereoisomers in moderate to good yields.

A new route to 1,2,3-triazole fused benzooxazepine and benzodiazepine analogues through metal-free intramolecular azide-olefin oxidative cycloaddition

A collection of 1,2,3-triazole fused benzooxazepine and benzodiazepine analogues was prepared by one pot azide substitution and intramolecular azide-olefin oxidative cycloaddition sequence under metal-free conditions.

Cascade Skeletal Rearrangement of Gold Carbene Intermediates: Synthesis of Medium-Sized Pyrimidine-Fused Benzolactones

A gold-catalyzed cyclization/cascade skeletal rearrangement of o-cyanophenylalkynones with 3-amino-benzo[d]-isoxazoles has been developed, which provides an approach for synthesizing medium-sized benzolactones. Based on the experimental results, we postul

Transition metal-free approach to azafluoranthene scaffolds by aldol condensation/[1+2+3] annulation tandem reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes

A transition metal-free aldol condensation/[1+2+3] annulation reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes has been developed for the general synthesis of azafluoranthenes. This domino reaction enables successive formation of three new bonds and two rings from readily accessible starting materials in a single operation. Furthermore, this methodology can also be utilized to construct chromeno[4,3-c]pyridines and benzo[c][2,6]naphthyridines in moderate yields.