D-Erythronolactone
Modify Date: 2024-01-09 22:32:29
D-Erythronolactone structure
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Common Name | D-Erythronolactone | ||
|---|---|---|---|---|
| CAS Number | 15667-21-7 | Molecular Weight | 118.088 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 277.1±7.0 °C at 760 mmHg | |
| Molecular Formula | C4H6O4 | Melting Point | 100-102ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 129.1±11.7 °C | |
| Name | d-erythronolactone |
|---|---|
| Synonym | More Synonyms |
| Density | 1.7±0.1 g/cm3 |
|---|---|
| Boiling Point | 277.1±7.0 °C at 760 mmHg |
| Melting Point | 100-102ºC(lit.) |
| Molecular Formula | C4H6O4 |
| Molecular Weight | 118.088 |
| Flash Point | 129.1±11.7 °C |
| Exact Mass | 118.026611 |
| PSA | 66.76000 |
| LogP | -2.07 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.580 |
| Storage condition | -20°C |
| Safety Phrases | 24/25 |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2932209090 |
| Precursor 8 | |
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| DownStream 4 | |
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CAS#:7425-21-0| HS Code | 2932209090 |
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| Summary | 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Evolution of enzymatic activities in the enolase superfamily: L-fuconate dehydratase from Xanthomonas campestris.
Biochemistry 45(49) , 14582-97, (2006) Many members of the mechanistically diverse enolase superfamily have unknown functions. In this report we use both genome (operon) context and screening of a library of acid sugars to assign the L-fuc... |
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Biosynthesis of ascorbate in yeast. Purification of L-galactono-1,4-lactone oxidase with properties different from mammalian L-gulonolactone oxidase.
Eur. J. Biochem. 127(2) , 391-6, (1982) An enzyme from Saccharomyces cerevisiae which catalyzes the reaction: L-galactonolactone + O2 leads to L-ascorbate + H2O2 has been purified 466-fold from the mitochondrial fraction of a yeast homogena... |
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Carbon-branched carbohydrate chirons: practical access to both enantiomers of 2-C-methyl-ribono-1,4-lactone and 2-C-methyl-arabinonolactone. Booth, K. V., et al.
Tetrahedron Asymmetry 20 , 2357-2367, (2009)
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| D-Erythronolactone |
| 2,3,4-Quinolinetriol |
| D-Erythronic g-lactone |
| 3,4-Dihydroxy-2-oxo-1,2-dihydro-chinolin |
| (3R,4R)-3,4-Dihydroxydihydrofuran-2(3H)-one |
| 2,4-Quinolinetriol |
| Carbostyril-3,4-diol |
| 1H-2-oxo-3,4-dihydroxyquinoline |
| D-Erythronic acid γ-lactone |
| D-Erythrono-1,4-lactone |
| Erythrono-1,4-lactone |
| (3R,4R)-3,4-Dihydroxydihydro-2(3H)-furanone |
| (3R,4R)-(-)-D-Erythronolactone |
| MFCD00077763 |
| 2(3H)-Furanone, dihydro-3,4-dihydroxy-, (3R,4R)- |
| D-Erythronic γ-Lactone |
| (3R,4R)-Dihydroxydihydro-2(3H)-furanone |
| 2-Oxo-3,4-dihydroxy-1,2-dihydroquinolin |
| 3,4-dihydroxy-dihydro-furan-2-one |
| 3,4-Dihydroxy-carbostyril |