Basic information Safety Supplier Related

4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE

Basic information Safety Supplier Related

4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE Basic information

Product Name:
4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE
Synonyms:
  • 2-Carboxy-5-oxo-5,6,7,8-tetrahydronaphthalene
  • 6-Carboxy-1-oxo-1,2,3,4-tetrahydronaphthalene, 5-Oxo-5,6,7,8-tetrahydro-2-naphthoic acid
  • 4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE
  • 4-[(4-METHYLPHENYL)SULPHONYL]PIPERIDINE HYDROCHLORIDE
  • 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid 96%
  • 5-Oxo-7,8-dihydro-6H-naphthalene-2-carboxylic Acid
  • 2-Naphthalenecarboxylic acid, 5,6,7,8-tetrahydro-5-oxo-
CAS:
3470-46-0
MF:
C11H10O3
MW:
190.2
Product Categories:
  • Benzocycles
Mol File:
3470-46-0.mol
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4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE Chemical Properties

Melting point:
230(dec.)
Boiling point:
230 °C/dec)
Density 
1.309±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.77±0.20(Predicted)
form 
solid
color 
Light brown
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Safety Information

Hazard Codes 
Xi,C
HazardClass 
IRRITANT
HS Code 
2902900000
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4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE Usage And Synthesis

Synthesis

144464-66-4

3470-46-0

Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate (320 mg, 1.57 mmol) was used as a raw material and dissolved in a solvent mixture of 6 mL of methanol and 3 mL of water. Subsequently, lithium hydroxide (331 mg, 7.88 mmol) was added. The reaction mixture was stirred at room temperature for 1 h. The progress of the reaction was monitored by thin-layer chromatography (TLC), and after confirming that the reaction was complete, the pH of the reaction solution was adjusted to 5 with 1 N hydrochloric acid solution.The reaction solution was concentrated by rotary evaporation and extracted with ethyl acetate (50 mL × 2). The ethyl acetate extracts were combined and the solvent was removed by rotary evaporation to afford the white solid product 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid (310 mg, 100% yield).

References

[1] Patent: CN104844471, 2017, B. Location in patent: Paragraph 0186; 0187; 0188

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