ChemicalBook--->CAS DataBase List--->103260-44-2

103260-44-2

103260-44-2 Structure

103260-44-2 Structure
IdentificationBack Directory
[Name]

ETHYL TETRAHYDROPYRAN-4-YL-ACETATE
[CAS]

103260-44-2
[Synonyms]

2-(4-oxanyl)butanoate
ethyl 2-(oxan-4-yl)acetate
Ethyl tetrahydropyranyl-4...
Ethyl tetrahydropyran-4-acetate
Ethyl tetrahydropyranyl-4-acetate
Ethyl 2-(tetrahydro-2H-pyran-4-yl)
ETHYL TETRAHYDROPYRAN-4-YL-ACETATE
Ethyl tetrahydro-2H-pyran-4-acetate
Ethyl 2-(4-Tetrahydropyranyl)acetate
tetrahydropyran-4-yl-acetate ethyl ester
ETHYL 2-(TETRAHYDRO-2H-PYRAN-4-YL)ACETATE
(Tetrahydropyran-4-yl)acetic acid ethyl ester
Pyran-4-acetic acid, tetrahydro-, ethyl ester
2H-Pyran-4-acetic acid, tetrahydro-, ethyl ester
[Molecular Formula]

C9H16O3
[MDL Number]

MFCD03788560
[MOL File]

103260-44-2.mol
[Molecular Weight]

172.22
Chemical PropertiesBack Directory
[Boiling point ]

73-75 0,2mm
[density ]

1.0268 g/cm3(Temp: 13.4 °C)
[refractive index ]

1.4572 (13.4℃)
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

103260-44-2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36-36/37/39-23
[Hazard Note ]

Irritant
[HS Code ]

2932990090
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL TETRAHYDROPYRAN-4-YL-ACETATE(103260-44-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl (tetrahydro-4H-pyran-4-ylidene)acetate

130312-00-4

ETHYL TETRAHYDROPYRAN-4-YL-ACETATE

103260-44-2

General procedure for the synthesis of ethyl tetrahydropyran-4-yl-acetate from ethyl 2-(dihydro-2H-pyran-4(3H)-ylidene)acetate: ethyl tetrahydro-4H-pyran-4-ylidene acetate (16.0 g, 94 mmol) was reacted with Pd/NH4COOH at 80 °C to give the colorless oily product ethyl tetrahydropyran-4-yl-acetate. Yield: 16.3 g (quantitative), mass spectral (MS) data: m/z 173.2 ([M + H]+).

[References]

[1] Journal of Medicinal Chemistry, 2004, vol. 47, # 25, p. 6255 - 6269
[2] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 23, p. 6309 - 6323
[3] Patent: US6340691, 2002, B1. Location in patent: Page column 66
[4] Patent: EP1147080, 2004, B1. Location in patent: Page 49
[5] Patent: WO2013/37960, 2013, A1. Location in patent: Page/Page column 76
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