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Tetrahydro-4H-pyran-4-one, 98%
CAS: 29943-42-8 | C5H8O2 | 100.117 g/mol
$81.07 - $1002.21
Chemical Identifiers
CAS | 29943-42-8 |
---|---|
Molecular Formula | C5H8O2 |
Molecular Weight (g/mol) | 100.117 |
MDL Number | MFCD00006581 |
InChI Key | JMJRYTGVHCAYCT-UHFFFAOYSA-N |
Synonym | tetrahydro-4h-pyran-4-one, 4-oxotetrahydropyran, tetrahydropyran-4-one, dihydro-2h-pyran-4 3h-one, 4h-pyran-4-one, tetrahydro, 4-thp, tetrahydro-2h-pyran-4-one, tetrahydro-pyran-4-one, 4-oxotetrahydopyran, tetrahydro-.gamma.-pyrone |
PubChem CID | 121599 |
IUPAC Name | oxan-4-one |
SMILES | C1COCCC1=O |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAA1901003
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Thermo Scientific Chemicals
A1901003 |
1 g |
Each for $81.07
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AAA1901006
|
Thermo Scientific Chemicals
A1901006 |
5 g |
Each for $221.92
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AAA1901014
|
Thermo Scientific Chemicals
A1901014 |
25 g |
Each for $1,002.21
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Description
It is employed in the preparation of 4-methoxytetrahydropyran-4-yl protecting group, synthesis of symmetric tetra substituted methanes. The methyl enol ether is a useful protecting agent for alcohols, e.g. in nucleotide synthesis, with the advantage over 3,4-Dihydro-2H-pyran. It is also employed in a study of the enantioselective alpha-aminoxylation of ketones with nitrosobenzene and L-proline in an ionic liquid. It undergoes condensation reactions in the preparation of dipeptides and spiroimidazolones. It is also employed in wittig reactions for the synthesis of Penicillins and in a ring of vitamin D3
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.
ApplicationsIt is employed in the preparation of 4-methoxytetrahydropyran-4-yl protecting group, synthesis of symmetric tetra substituted methanes. The methyl enol ether is a useful protecting agent for alcohols, e.g. in nucleotide synthesis, with the advantage over 3,4-Dihydro-2H-pyran. It is also employed in a study of the enantioselective alpha-aminoxylation of ketones with nitrosobenzene and L-proline in an ionic liquid. It undergoes condensation reactions in the preparation of dipeptides and spiroimidazolones. It is also employed in wittig reactions for the synthesis of Penicillins and in a ring of vitamin D3
Solubility
Very soluble in water.
Notes
Store away from strong bases and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
Chemical Identifiers
29943-42-8 | |
100.117 | |
JMJRYTGVHCAYCT-UHFFFAOYSA-N | |
121599 | |
C1COCCC1=O |
C5H8O2 | |
MFCD00006581 | |
tetrahydro-4h-pyran-4-one, 4-oxotetrahydropyran, tetrahydropyran-4-one, dihydro-2h-pyran-4 3h-one, 4h-pyran-4-one, tetrahydro, 4-thp, tetrahydro-2h-pyran-4-one, tetrahydro-pyran-4-one, 4-oxotetrahydopyran, tetrahydro-.gamma.-pyrone | |
oxan-4-one |
Specifications
29943-42-8 | |
165°C to 167°C | |
C5H8O2 | |
MFCD00006581 | |
106463 | |
Very soluble in water. | |
C1COCCC1=O | |
100.117 | |
100.12 | |
Tetrahydro-4H-pyran-4-one |
1.084 | |
62°C (144°F) | |
1.453 | |
1 g | |
tetrahydro-4h-pyran-4-one, 4-oxotetrahydropyran, tetrahydropyran-4-one, dihydro-2h-pyran-4 3h-one, 4h-pyran-4-one, tetrahydro, 4-thp, tetrahydro-2h-pyran-4-one, tetrahydro-pyran-4-one, 4-oxotetrahydopyran, tetrahydro-.gamma.-pyrone | |
JMJRYTGVHCAYCT-UHFFFAOYSA-N | |
oxan-4-one | |
121599 | |
98% |
Safety and Handling
GHS H Statement
H227
Combustible liquid.
P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
H226
DOTInformation : Hazard Class: 3; Packaging Group: III
EINECSNumber : 249-967-2
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only