Tetrahydropyran, 98+%, Thermo Scientific Chemicals
Tetrahydropyran, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Tetrahydropyran, 98+%, Thermo Scientific Chemicals

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Quantity:
500 mL
100 mL
Catalog number A13392.AP
also known as A13392-AP
Price (USD)/ Each
175.65
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206.00 
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Quantity:
500 mL
Request bulk or custom format
Price (USD)/ Each
175.65
Online exclusive
206.00 
Save 30.35 (15%)
Add to cart
Tetrahydropyran, 98+%, Thermo Scientific Chemicals
Catalog numberA13392.AP
Price (USD)/ Each
175.65
Online exclusive
206.00 
Save 30.35 (15%)
-
Add to cart
Chemical Identifiers
IUPAC Nameoxane
Molecular FormulaC5H10O
InChI KeyDHXVGJBLRPWPCS-UHFFFAOYSA-N
SMILESC1CCOCC1
Molecular Weight (g/mol)86.13
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SpecificationsSpecification SheetSpecification Sheet
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.

Applications
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.

Solubility
It is soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from Oxidizing agents, Strong acids. May form peroxides in the absence of inhibitors. Light sensitive
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.