Results 311 to 320 of about 72,007 (341)
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The Methyl Ethers of D-Galactose
1951Publisher Summary This chapter discusses methyl ethers of D -galactose. The 2,3,4,6-tetramethyl- D -galactopyranos is obtained by the full methylation of the methyl α- or β- D -galactopyranosides, followed by acid hydrolysis of the products.
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Relative Permittivity Measurements of Trifluoromethyl Methyl Ether and Pentafluoroethyl Methyl Ether
Journal of Chemical & Engineering Data, 2007The relative permittivities (er) of trifluoromethyl methyl ether (HFE 143a) and pentafluoroethyl methyl ether (HFE 245mc) were measured as a function of temperature and pressure: (303 to 383) K and (1.5 to 31.6) MPa for HFE 143a and (313 to 323) K and (1.5 to 28.4) MPa for HFE 245mc.
Wayne Eltringham, Owen J. Catchpole
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Journal of Chemical & Engineering Data, 2003
PVT properties are presented for both the gas-phase and liquid-phase, vapor pressures and saturated-liquid densities for hydrofluoroether (HFE) refrigerants, trifluoromethyl methyl ether (CF3OCH3) and pentafluoroethyl methyl ether (C2F5OCH3), that were obtained with a Burnett apparatus and a vibrating-tube densimeter.
Yohei Kayukawa +4 more
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PVT properties are presented for both the gas-phase and liquid-phase, vapor pressures and saturated-liquid densities for hydrofluoroether (HFE) refrigerants, trifluoromethyl methyl ether (CF3OCH3) and pentafluoroethyl methyl ether (C2F5OCH3), that were obtained with a Burnett apparatus and a vibrating-tube densimeter.
Yohei Kayukawa +4 more
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2007
[13057-19-7] C2H5IO (MW 171.97) InChI = 1S/C2H5IO/c1-4-2-3/h2H2,1H3 InChIKey = UUSXSNJAQDJKCG-UHFFFAOYSA-N (reactive methoxymethylating agent for phosphorus,1 carbon,2 oxygen,3 and nitrogen4 nucleophiles; iodomethylating agent for aromatic systems5) Alternate Name: iodomethoxymethane. Physical Data: bp 122 °C (dec)
Michael E. Jung +2 more
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[13057-19-7] C2H5IO (MW 171.97) InChI = 1S/C2H5IO/c1-4-2-3/h2H2,1H3 InChIKey = UUSXSNJAQDJKCG-UHFFFAOYSA-N (reactive methoxymethylating agent for phosphorus,1 carbon,2 oxygen,3 and nitrogen4 nucleophiles; iodomethylating agent for aromatic systems5) Alternate Name: iodomethoxymethane. Physical Data: bp 122 °C (dec)
Michael E. Jung +2 more
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2005
[4885-02-3] C2H4Cl2O (MW 114.96) InChI = 1S/C2H4Cl2O/c1-5-2(3)4/h2H,1H3 InChIKey = GRTGGSXWHGKRSB-UHFFFAOYSA-N (carbon monoxide equivalent in reactions with boranes and borinates; formylating reagent for aromatic compounds and vinylsilanes; formation of α-keto acid chlorides) Alternate Name: dichloromethoxymethane; DCME.
Kevin E. Henegar +2 more
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[4885-02-3] C2H4Cl2O (MW 114.96) InChI = 1S/C2H4Cl2O/c1-5-2(3)4/h2H,1H3 InChIKey = GRTGGSXWHGKRSB-UHFFFAOYSA-N (carbon monoxide equivalent in reactions with boranes and borinates; formylating reagent for aromatic compounds and vinylsilanes; formation of α-keto acid chlorides) Alternate Name: dichloromethoxymethane; DCME.
Kevin E. Henegar +2 more
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CRYSTALLINE VITAMIN A METHYL ETHER
Journal of the American Chemical Society, 1946A. R. Hanze +3 more
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2001
[13057-17-5] C2H5BrO (MW 124.96) InChI = 1S/C2H5BrO/c1-4-2-3/h2H2,1H3 InChIKey = JAMFGQBENKSWOF-UHFFFAOYSA-N (alkylating agent; formaldehyde equivalent;1-8 alcohol protecting group9-14) Alternate Name: BMME. Physical Data: bp 87 °C; d 1.531 g cm−3.
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[13057-17-5] C2H5BrO (MW 124.96) InChI = 1S/C2H5BrO/c1-4-2-3/h2H2,1H3 InChIKey = JAMFGQBENKSWOF-UHFFFAOYSA-N (alkylating agent; formaldehyde equivalent;1-8 alcohol protecting group9-14) Alternate Name: BMME. Physical Data: bp 87 °C; d 1.531 g cm−3.
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2005
[3492-44-2] C2H4Br2O (MW 203.86) InChI = 1S/C2H4Br2O/c1-5-2(3)4/h2H,1H3 InChIKey = HDMDJEKUPKOGNK-UHFFFAOYSA-N (brominating reagent, reagent to effect conversions at the anomeric center of carbohydrates) Physical Data: bp 32–33 °C/13 mm Hg.
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[3492-44-2] C2H4Br2O (MW 203.86) InChI = 1S/C2H4Br2O/c1-5-2(3)4/h2H,1H3 InChIKey = HDMDJEKUPKOGNK-UHFFFAOYSA-N (brominating reagent, reagent to effect conversions at the anomeric center of carbohydrates) Physical Data: bp 32–33 °C/13 mm Hg.
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Carcinogenicity of Methyl Ether Compounds
New England Journal of Medicine, 1973B K, Leong, H N, MacFarland, W H, Reese
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