82652-12-8

Basic information

• Product Name: 4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE
• Synonyms: 1-(3-FLUOROBENZOYL)DIMETHYLSULFONE;1-(3-FLUOROBENZOYL)DIMETHYLSULPHONE;1-(3-FLUOROPHENYL)-2-(METHYLSULFONYL)ETHANONE;3'-FLUORO-2-METHYLSULFONYLACETOPHENONE;3'-FLUORO-2-METHYLSULPHONYLACETOPHENONE;4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE;1-(3-Fluorophenyl)-2-(methylsulphonyl)ethanone;1-(3-Fluorophenyl)-2-(methylsulphonyl)ethan-1-one
• CAS NO: 82652-12-8
• Molecular Formula: C₉H₉FO₃S
• Molecular Weight: 216.23
• Mol File: 82652-12-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: 81-83°C
• Boiling Point: 414.3 ºC at 760 mmHg
• Flash Point: 204.4 ºC
• Appearance: /
• Density: 1.328 g/cm³
• Vapor Pressure: 3.47E-05mmHg at 25°C
• CAS DataBase Reference: 4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE(82652-12-8)
• EPA Substance Registry System: 4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE(82652-12-8)

Safety Data

• Hazard Codes: C,Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 82652-12-8(Hazardous Substances Data)

Usage

General Description

"4-(Methylsulfonylamino)benzylamine hydrochloride" is a chemical compound that contains a benzylamine group with a methylsulfonylamino substitution. It is commonly used in the synthesis of pharmaceutical compounds and organic chemicals. 4-(METHYLSULFONYLAMINO)BENZYLAMINE HYDROCHLORIDE has potential applications in the field of medicinal chemistry and drug discovery, as well as in research and development of new materials. The hydrochloride salt form of this compound increases its stability and solubility in water, making it more suitable for various applications in the pharmaceutical industry. Overall, 4-(Methylsulfonylamino)benzylamine hydrochloride holds promise for further research and development in the field of chemistry and medicine.

InChI:InChI=1/C8H12N2O2S.ClH/c1-13(11,12)10-8-4-2-7(6-9)3-5-8;/h2-5,10H,6,9H2,1H3;1H

Upstream product

• 2561-17-3 1-ethynyl-3-fluoro-benzene 
• 67-71-0 dimethylsulfone 
• 455-68-5 methyl 3-fluorobenzoate 
• 350-51-6 3-fluorostyrene 

Downstream Products

• 1599463-30-5 (Z)-N-(1-(3-fluorophenyl)-2-(methylsulfonyl)vinyl)acetamide 

Relevant articles and documents

Visible-light-promoted aerobic oxidative synthesis of β-ketosulfones under photocatalyst-free conditions

A simple and convenient visible-light-mediated method has been developed for the construction of β-ketosulfones via aerobic oxidative difunctionalization of alkynes with arylazo sulfones and dioxygen in air under photocatalyst-free conditions. The present photochemical methodology provides a facile and attractive protocol to construct a series of β-ketosulfones in moderate to good yields.

Photocatalyst-Free Visible Light-Induced Synthesis of β-Oxo Sulfones via Oxysulfonylation of Alkenes with Arylazo Sulfones and Dioxygen in Air

A catalyst-free strategy has been established for the synthesis of β-oxo sulfones via visible light-induced oxysulfonylation of alkenes with arylazo sulfones with dioxygen in air. The present photoinduced transformation proceeds smoothly at room temperature in the absence of an external photosensitizer, which not only provides a mild and efficient approach to various β-oxo sulfones, but also opens a different reaction mode for the photochemical reaction of arylazo sulfones.