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(S)-(+)-5-(hidroximetil)-2-pirrolidinona, 98 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

(S)-(+)-5-(hidroximetil)-2-pirrolidinona, 98 %, Thermo Scientific Chemicals

Name: (S)-(+)-5-(hidroximetil)-2-pirrolidinona, 98 %, Thermo Scientific Chemicals
SKU: L18359.03
Price: 41.40 EUR

CAS: 17342-08-4 | C5H9NO2 | 115.132 g/mol

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Cantidad:

1 g

5 g

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Número de catálogo L18359.03

también denominado L18359-03

Precio (EUR)

41,40

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Cantidad:

1 g

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Precio (EUR)

41,40

Each

Identificadores químicos

CAS17342-08-4

IUPAC Name(5S)-5-(hydroxymethyl)pyrrolidin-2-one

Molecular FormulaC5H9NO2

InChI KeyHOBJEFOCIRXQKH-BYPYZUCNSA-N

SMILESOC[C@@H]1CCC(=O)N1

Especificaciones Specification Sheet

Hoja de especificaciones

FormCrystals or powder or crystalline powder

Water Content (Karl Fischer Titration)≤1.5%

Appearance (Color)White to pale cream to pale brown

Optical Rotation30.5 ± 0.1? (C=2 in ethanol)

Assay (HPLC)≥97.5%

(S)-(+)-5-(Hydroxymethyl)-2-pyrrolidinone serves as a building block in the synthesis of (R)- and (S)-diaminovaleric acids1 and of 5-azasemicorrin bidentate nitrogen ligands for enantioselective catalysis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
La (S)-(+)-5-(hidroximetil)-2-pirrolidinona sirve como compuesto básico en la síntesis de ácidos (R)- y (S)-diaminovaléricos1 y de ligantes de nitrógeno 5-azasemicorrin bidentado para catálisis enantioselectiva.

Solubilidad
Soluble en agua.

Notas
Almacenar en un lugar fresco. Mantener el recipiente bien cerrado en un lugar seco y bien ventilado.

RUO – Research Use Only

General References:

Richard B. Silverman.; Mark A. Levy. Syntheses of (S)-5-substituted 4-aminopentanoic acids: a new class of .gamma.-aminobutyric acid transaminase inactivators. J. Org. Chem. 1980, 45 (5), 815-818.
John K. Thottathil, Jerome L. Moniot, Richard H. Mueller, Michael K. Y. Wong, Thomas P. Kissick. Conversion of L-pyroglutamic acid to 4-alkyl-substituted L-prolines. The synthesis of trans-4-cyclohexyl-L-proline. J. Org. Chem. 1986, 51 (16), 3140-3143.