| Identification | Back Directory | [Name]
(-)-1,4-ANHYDRO-L-THREITOL | [CAS]
4358-64-9 | [Synonyms]
L-THREITAN
ERYTHRITAN
Meso-3,4-Dihydr
oxolane-3,4-diol
cis-Oxolane-3,4-diol
1,4-Anhydroerythrotole
Erythritol-1,4-anhydride
cis-3,4-Dihydroxyoxolane
1,4-Anhydroerythritol 95%
1,4-anhydride - erythritol
(-)-1,4-ANHYDRO-L-THREITOL
cis-tetrahydrofuran-3,4-diol
1,4-Anhydroerythritol min. 98%
(3S)-Tetrahydrofuran-3α,4β-diol
(3R,4S)-Tetrahydro-3,4-furandiol
(3R,4S)-Tetrahydrofuran-3,4-diol
(3S,4R)-Tetrahydro-3,4-furandiol
(3S,4R)-Tetrahydrofuran-3,4-diol
1,4-ANHYDROERYTHRITOL 98.0+%(GC)
cis-3,4-Dihydroxytetrahydrofuran
(3S,4S)-TETRAHYDRO-FURAN-3,4-DIOL | [EINECS(EC#)]
224-433-1 | [Molecular Formula]
C4H8O3 | [MDL Number]
MFCD00075211 | [MOL File]
4358-64-9.mol | [Molecular Weight]
104.1 |
| Chemical Properties | Back Directory | [Melting point ]
173-174 °C | [Boiling point ]
160-165 °C(Press: 0.17 Torr) | [density ]
1.27 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.477(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,2-8°C | [form ]
powder to lump to clear liquid | [pka]
13.66±0.40(Predicted) | [color ]
White or Colorless to Almost white or Almost colorless | [InChI]
InChI=1/C4H8O3/c5-3-1-7-2-4(3)6/h3-6H,1-2H2/t3-,4+ | [InChIKey]
SSYDTHANSGMJTP-ZXZARUISNA-N | [SMILES]
O1C[C@H](O)[C@H](O)C1 |&1:2,4,r| |
| Hazard Information | Back Directory | [Uses]
1,4-Anhydroerythritol is a tetrahydrofuran derivative used as a heterocyclic building block in epoxy resins and other polymers. 1,4-Anhydroerythritol is also used in the preparation of nucleotide anal
ogs as potential antiviral and anticancer agents. | [General Description]
1,4-Anhydroerythritol is a cyclic vicinal diol. 1,4-Anhydroerythritol undergoes hydrodeoxygenation over tungsten oxide-palladium catalysts to yield 3-hydroxytetrahydrofuran. | [Synthesis]
The round-bottom distillation flask was preheated to 240 ℃, 50 g of erythritol crystals and 0.5 g of Amberlyst131 resin were added, the pressure of the distillation flask was adjusted to 0.5 bar, and the reaction was carried out for 2.5 h. The reaction |
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