Tetrahidropirano, +98 %, Thermo Scientific Chemicals
Tetrahidropirano, +98 %, Thermo Scientific Chemicals
Tetrahidropirano, +98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Tetrahidropirano, +98 %, Thermo Scientific Chemicals

CAS: 142-68-7 | C5H10O | 86.134 g/mol
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Cantidad:
100 mL
500 mL
Número de catálogo A13392.AE
también denominado A13392-AE
Precio (EUR)
48,30
Each
Cantidad:
100 mL
Pedido a granel o personalizado
Precio (EUR)
48,30
Each
Identificadores químicos
CAS142-68-7
IUPAC Nameoxane
Molecular FormulaC5H10O
InChI KeyDHXVGJBLRPWPCS-UHFFFAOYSA-N
SMILESC1CCOCC1
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EspecificacionesSpecification SheetHoja de especificaciones
Refractive Index1.4190-1.4230 @ 20?C
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.0%
FormLiquid
Identification (FTIR)Conforms
It is is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and dyestuff. They are also used as important solvents, as chemical intermediate and as monomer for ring-opening polymerization.

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
Es una importante materia prima e intermediario utilizado en síntesis orgánica, productos farmacéuticos, agroquímicos y colorantes. También se utiliza como disolvente importante, intermediario químico y monómero para la polimerización de apertura de anillo.

Solubilidad
Soluble en agua.

Notas
Almacenar en un lugar fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Mantener alejado de agentes oxidantes y ácidos fuertes. Puede formar peróxidos en ausencia de inhibidores. Sensible a la luz
RUO – Research Use Only

General References:

  1. AB Smith.; S Sasho.; BA Barwis.; P Sprengeler. Design and synthesis of a tetrahydropyran-based inhibitor of mammalian ribonucleotide reductase. Bioorganic & Medicinal Chemistry Letters. 1998, 8,(22), 3133-3136.
  2. HK Hsieh.; TH Lee.; JP Wang.; JJ Wang.; CN Lin. Synthesis and anti-inflammatory effect of chalcones and related compounds. Pharmaceutical research. 1998, 15,(1), 39-46.
  3. Alcohols have been protected as their tetrahydropyranyl ethers under non-acidic, free radical conditions: Synlett, 207 (1995); cf 3,4-Dihydro-2H-pyran, L02731.