ChemicalBook--->CAS DataBase List--->17852-67-4

17852-67-4

17852-67-4 Structure

17852-67-4 Structure
IdentificationBack Directory
[Name]

4-(Methylsulfonyl)phenylhydrazine hydrochloride
[CAS]

17852-67-4
[Synonyms]

TIMTEC-BB SBB003335
4-Hydrazino-1-(methylsulphonyl)benzene
4-METHYLSULPHONYLPHENYLHYDRAZINE HYDROCHLORIDE
4-(Methylsulfonyl)phenylhydrazine hydrochloride
(4-Methanesulfonyl-phenyl)-hydrazine hydrochloride
4-(Methylsulfonyl)phenylhydrazine hydrochloride,95%
4-Hydrazino-1-(methylsulphonyl)benzene hydrochloride
4-(Methylsulfonyl)phenylhydrazine hydrochloride, 95% 2.5GR
1-Hydrazino-4-(methylsulphonyl)benzene hydrochloride, 4-Hydrazinophenyl methyl sulphone hydrochloride
[Molecular Formula]

C7H11ClN2O2S
[MDL Number]

MFCD00216494
[MOL File]

17852-67-4.mol
[Molecular Weight]

222.69
Chemical PropertiesBack Directory
[Appearance]

off-white to light yellow crystalline powder
[Melting point ]

202 °C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Crystalline Powder
[color ]

Off-white to light yellow
[Water Solubility ]

SOLUBLE
Hazard InformationBack Directory
[Chemical Properties]

off-white to light yellow crystalline powder
[Synthesis]

4-Methylsulfonylaniline

5470-49-5

4-(Methylsulfonyl)phenylhydrazine hydrochloride

17852-67-4

General procedure for the synthesis of 4-(methylsulfonyl)phenylhydrazine hydrochloride from 4-methylsulfonylaniline: 100 mL of hydrochloric acid was added to a 500 mL four-necked flask, and the temperature inside the flask was cooled to -10 °C or lower by passing the flask through an ice-water bath and ensuring that the temperature did not exceed -10 °C. Subsequently, 10.27 g (0.06 mol) of 4-(methylsulfonyl)aniline was added and dissolved. After the exothermic reaction ceased, 4.47 g (0.065 mol) of sodium nitrite was slowly added and 30 g of distilled water was added dropwise over a period of 1 hour while keeping the temperature of the flask below -10°C. After completion of the addition, the addition of 67.7 g (0.30 mol) of tin chloride dihydrate dissolved in 60 mL of hydrochloric acid was continued dropwise over 1 h while the reaction temperature was strictly controlled at -10 °C or lower. Upon completion of the reaction, the solid product was collected by filtration and dried at 60 °C for 12 h using a vacuum drier to afford 4-(methylsulfonyl)phenylhydrazine hydrochloride (Intermediate G1). This step was based on a 67.9 mol% yield of 4-(methylsulfonyl)phenylhydrazine.

[References]

[1] Patent: JP2018/95798, 2018, A. Location in patent: Paragraph 0081; 0084
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Safety Statements ]

22-24/25
[HS Code ]

29280000
Spectrum DetailBack Directory
[Spectrum Detail]

4-(Methylsulfonyl)phenylhydrazine hydrochloride(17852-67-4)1HNMR
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