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Assay
98%
optical activity
[α]20/D −144°, c = 1 in H2O
mp
41-43 °C (lit.)
storage temp.
2-8°C
SMILES string
OC[C@H]1OC(=O)C=C1
InChI
1S/C5H6O3/c6-3-4-1-2-5(7)8-4/h1-2,4,6H,3H2/t4-/m0/s1
InChI key
AWNLUIGMHSSXHB-BYPYZUCNSA-N
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Application
(S)-(−)-5-Hydroxymethyl-2(5H)-furanone can be used as a starting material in the preparation of:
- Partially saturated heterocycles via a diastereoselective ring chain formation.
- A natural product named (+)-muscarine.
- 3′-Ethynylthymidine as a possible antiviral agent.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Synthesis of (+)-muscarine from (S)-(-)-5-hydroxymethyl-2 (5H)-furanone
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Synthesis of 3′-ethynylthymidine, 3′-vinylthymidine and 3′-bromovinylthymidine as potential antiviral agents
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Highly diastereoselective ring chain transformation of butonolides to 5-(a-hydroxyalkyl) pyrazolidin-3-ones
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