ChemicalBook--->CAS DataBase List--->4972-31-0

4972-31-0

4972-31-0 Structure

4972-31-0 Structure
IdentificationBack Directory
[Name]

1-(PHENYLSULFINYL)PIPERIDINE 97
[CAS]

4972-31-0
[Synonyms]

1-(Phenylsulfinyl)piperidine
1-BENZENESULFINYLPIPERIDINE 97%
Piperidine, 1-(phenylsulfinyl)-
1-(Phenylsulfinyl)piperidine 97%
1-(PHENYLSULFINYL)PIPERIDINE 97
1-(Phenylsulfinyl)piperidine,1-Benzenesulfinylpiperidine
[Molecular Formula]

C11H15NOS
[MDL Number]

MFCD05155800
[MOL File]

4972-31-0.mol
[Molecular Weight]

209.31
Chemical PropertiesBack Directory
[Melting point ]

84-88 °C (lit.)
[Boiling point ]

354.2±25.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[pka]

-2.48±0.20(Predicted)
[InChI]

InChI=1S/C11H15NOS/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1,3-4,7-8H,2,5-6,9-10H2
[InChIKey]

LBRJCAJLGAXDKP-UHFFFAOYSA-N
[SMILES]

N1(S(C2=CC=CC=C2)=O)CCCCC1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

1-(Phenylsulfinyl)piperidine can be used prepared aminoglycoside antibiotics.
[Uses]

Reagent for:• ;Selective glycosylation1• ;Mannopyranolsylations2• ;Design of enzyme stabilizers3Reagent for synthesis of:• ;Glycan array for affinity studies with influenza hemagglutinins†• ;Orthogonal protecting groups for preparation of highly branched oligosaccharides4• ;Tetrasaccharide repeating units related to E. Coli 78 O-antigenic polysaccharides5
[Uses]

Reagent for:
  • Selective glycosylation
  • Mannopyranolsylations
  • Design of enzyme stabilizers

Reagent for synthesis of:
  • Glycan array for affinity studies with influenza hemagglutinins?
  • Orthogonal protecting groups for preparation of highly branched oligosaccharides
  • Tetrasaccharide repeating units related to E. Coli 78 O-antigenic polysaccharides
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 49, p. 1931, 1984 DOI: 10.1021/jo00185a017
Chemical and Pharmaceutical Bulletin, 28, p. 134, 1980 DOI: 10.1248/cpb.28.134
Spectrum DetailBack Directory
[Spectrum Detail]

1-(PHENYLSULFINYL)PIPERIDINE 97(4972-31-0)1HNMR
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