Ethoxymethaniminium chloride
Ethoxymethaniminium chloride structure
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Common Name | Ethoxymethaniminium chloride | ||
|---|---|---|---|---|
| CAS Number | 16694-46-5 | Molecular Weight | 109.555 | |
| Density | 0.88g/cm3 | Boiling Point | 31.7ºC at 760mmHg | |
| Molecular Formula | C3H8ClNO | Melting Point | 75ºC | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Purines, pyrimidines, and imidazoles. XL. A new synthesis of a D-ribofuranosylamine derivative and its use in the synthesis of pyrimidine and imidazole nucleosides.
J. Chem. Soc. Perkin Trans. I 16 , 1720-31, (1973)
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Synthesis of the S-Triazine System. Iii. 1 Trimerization of Imidates. Schaefer FC and Peters GA.
J. Org. Chem. 26(8) , 2771-84, (1961)
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Purines, pyrimidines, and imidazoles. Part XLI. Glycofuranosylamines derived from D-xylose, D-glucose, D-mannose, and L-rhamnose and their use in the synthesis of pyrimidine and imidazole nucleosides. Cusack NJ, et al.
J. Chem. Soc. Perkin Trans. I , 73-81, (1974)
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Purines, pyrimidines, and imidazoles part 54. Interconversion of some intermediates in the de novo biosynthesis of purine nucleotides. Cusack NJ, et al.
J. Chem. Soc. Perkin Trans. I , 2316-21, (1980)
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Rhodd EH and von Richter V.
Chemistry of Organic Compounds: Pt. B. Aliphatic compounds , (1951), 551
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