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128263-66-1

128263-66-1 Structure

128263-66-1 Structure
IdentificationBack Directory
[Name]

4-(METHYLSULFONYLAMINO)BENZYLAMINEHYDROCHLORIDE
[CAS]

128263-66-1
[Synonyms]

4-(Methylsulfonylamino)benzylamine, HCl
N-(4-(AMinoMethyl)phenyl)MethanesulfonaMide hydrochloride
N-[4-(Aminomethyl)phenyl]methanesulphonamide hydrochloride
N-[4-(Aminomethyl)phenyl]methanesulphonamide hydrochloride 95+%
Methanesulfonamide, N-[4-(aminomethyl)phenyl]-, hydrochloride (1:1)
4-(Methylsulfonylamino)benzylamine hydrochloride(Methylsulfonylamino)Benzylaminehydrochloride
4-[(Methylsulphonyl)amino]benzylamine hydrochloride, 4-(Methylsulphonamido)benzylamine hydrochloride
[Molecular Formula]

C8H13ClN2O2S
[MDL Number]

MFCD06245516
[MOL File]

128263-66-1.mol
[Molecular Weight]

236.72
Chemical PropertiesBack Directory
[Melting point ]

>275℃ (dec.)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319
[Precautionary statements ]

P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312
[HazardClass ]

IRRITANT
[HS Code ]

2935909099
Spectrum DetailBack Directory
[Spectrum Detail]

4-(METHYLSULFONYLAMINO)BENZYLAMINEHYDROCHLORIDE (128263-66-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Carbamic acid, N-[[4-[(methylsulfonyl)amino]phenyl]methyl]-, 1,1-dimethylethyl ester

238427-63-9

4-(METHYLSULFONYLAMINO)BENZYLAMINEHYDROCHLORIDE

128263-66-1

Step 4: Synthesis of 4-methanesulfonylaminobenzylcarbamate hydrochloride; To a 50 mL single-necked round-bottomed flask was added tert-butyl 4-methanesulfonylaminobenzylcarbamate (1.2 g, 4.0 mmol) and 30 mL of 1,4-dioxane. Concentrated hydrochloric acid (2 mL) was slowly added to the solution and the reaction was stirred for 4 hours at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove the solvent. The resulting solid was washed with ethyl acetate and separated by filtration through a glass filter. Finally, the collected solid was dried in air to afford the target product 4-methylsulfonylaminobenzylamine hydrochloride (0.947 g, 100% yield).

[References]

[1] Patent: WO2006/98554, 2006, A1. Location in patent: Page/Page column 44
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