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Thermo Scientific Chemicals
Tetrahydropyran, 98+%
CAS: 142-68-7 | C5H10O | 86.134 g/mol
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Catalog number A13392.AE
also known as A13392-AE
Price (USD)
52.65
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57.80Save 5.15
Each
Quantity:
100 mL
Price (USD)
52.65
Online exclusive
57.80Save 5.15
Each
Chemical Identifiers
CAS142-68-7
IUPAC Nameoxane
Molecular FormulaC5H10O
InChI KeyDHXVGJBLRPWPCS-UHFFFAOYSA-N
SMILESC1CCOCC1
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Specifications
Specification Sheet
Specification SheetRefractive 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
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:
- 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.
- 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.
- Alcohols have been protected as their tetrahydropyranyl ethers under non-acidic, free radical conditions: Synlett, 207 (1995); cf 3,4-Dihydro-2H-pyran, L02731.