Results 251 to 260 of about 64,940 (304)
Some of the next articles are maybe not open access.
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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Total synthesis of (±)-shonanyl methyl ether and (±)-ferruginyl methyl ether
Tetrahedron Letters, 1989Abstract An efficient reductive methylation of the tricyclic ketone 12 in anhydrous ammonia provided the β,γ-unsaturated ketone 15 in high yield which was subsequently converted into (±)-shonanyl methyl ether ( 3 ) and (±)-ferruginyl methyl ether ( 6 ).
Manuka Ghosal +2 more
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Fluid Phase Equilibria, 2001
Abstract Thermodynamic properties of two fluorinated ethers, that meet the criteria of the potential new-generation refrigerants with considerably low global warming potential (GWP) and the zero ozone depletion potential (ODP), are studied in the present paper. The recommended candidates are pentafluoroethyl methyl ether, CF 3 CF 2 OCH 3 (245cbEβγ),
Januarius V. Widiatmo, Koichi Watanabe
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Abstract Thermodynamic properties of two fluorinated ethers, that meet the criteria of the potential new-generation refrigerants with considerably low global warming potential (GWP) and the zero ozone depletion potential (ODP), are studied in the present paper. The recommended candidates are pentafluoroethyl methyl ether, CF 3 CF 2 OCH 3 (245cbEβγ),
Januarius V. Widiatmo, Koichi Watanabe
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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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PGF2α 15-methyl ether methyl ester
Prostaglandins, 1974Abstract The isolation, structure elucidation, total synthesis, and biological activity of PGF 2 α 15-methyl ether methyl ester are described.
Gilbert A. Youngdale, Frank H. Lincoln
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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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2001
[107-30-2] C2H5ClO (MW 80.51) InChI = 1S/C2H5ClO/c1-4-2-3/h2H2,1H3 InChIKey = XJUZRXYOEPSWMB-UHFFFAOYSA-N (used for the protection of alcohols, phenols, acids, amines, β-keto esters and thiols. A one-carbon synthon for alkylation of aromatics and active methylene derivatives) Alternate Names: methoxymethyl chloride ...
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[107-30-2] C2H5ClO (MW 80.51) InChI = 1S/C2H5ClO/c1-4-2-3/h2H2,1H3 InChIKey = XJUZRXYOEPSWMB-UHFFFAOYSA-N (used for the protection of alcohols, phenols, acids, amines, β-keto esters and thiols. A one-carbon synthon for alkylation of aromatics and active methylene derivatives) Alternate Names: methoxymethyl chloride ...
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Journal of the Chemical Society D: Chemical Communications, 1969
T. Ohmoto, S. Natori
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T. Ohmoto, S. Natori
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