Identification | More | [Name]
(R)-(+)-Glycidol | [CAS]
57044-25-4 | [Synonyms]
OXIRANEMETHANOL, (2R)- (R)-(+)-2,3-EPOXY-1-PROPANOL (R)-(+)-GLYCIDOL (R)-GLYCIDOL R(+)-OXIRANE-2-METHANOL (R)-Oxiranemethanol (r)-oxiranemethano (R)-(+)-GLYCIDOL, 97% (98% EE/GLC) R-Glycidoe (R)-GLYCIDOL,99% (R)-3-Hydroxy-1,2-epoxypropane (R)-(+)-GLYCIDOL ((R)-(+)-2,3-EPOXY-1-PROPANOL) (2R)-Oxirane-2-methanol (R)-2-Hydroxymethyloxirane | [EINECS(EC#)]
404-660-4 | [Molecular Formula]
C3H6O2 | [MDL Number]
MFCD00074873 | [Molecular Weight]
74.08 | [MOL File]
57044-25-4.mol |
Chemical Properties | Back Directory | [Appearance]
Colorless to light yellow liqui | [Boiling point ]
56-57 °C11 mm Hg(lit.)
| [density ]
1.116 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.43(lit.)
| [Fp ]
178 °F
| [storage temp. ]
2-8°C
| [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [Water Solubility ]
Completely miscible in water | [form ]
neat | [pka]
14.62±0.10(Predicted) | [color ]
Colorless to Light yellow | [optical activity]
[α]23/D +15°, neat | [BRN ]
79782 | [Stability:]
Moisture Sensitive | [InChIKey]
CTKINSOISVBQLD-GSVOUGTGSA-N | [CAS DataBase Reference]
57044-25-4(CAS DataBase Reference) | [NIST Chemistry Reference]
Oxiranemethanol, (R)-(57044-25-4) |
Safety Data | Back Directory | [Hazard Codes ]
T,E | [Risk Statements ]
R45:May cause cancer. R60:May impair fertility. R2:Risk of explosion by shock, friction, fire or other sources of ignition. R21/22:Harmful in contact with skin and if swallowed . R23:Toxic by inhalation. R34:Causes burns. R68:Possible risk of irreversible effects. R41:Risk of serious damage to eyes. R37/38:Irritating to respiratory system and skin . | [Safety Statements ]
S53:Avoid exposure-obtain special instruction before use . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
UN 2922 8/PG 2
| [WGK Germany ]
3
| [RTECS ]
RR0508000
| [F ]
10-21 | [HazardClass ]
6.1 | [PackingGroup ]
Ⅲ | [HS Code ]
29109000 |
Hazard Information | Back Directory | [Chemical Properties]
Colorless to light yellow liqui | [Uses]
(R)-(+)-Glycidol may be used in the following synthesis:
- heteroarylpropane-2,3-diols, useful for combinatorial oligomer synthesis
- enantiomerically pure (2S,3S)- and (2S,3R)-threoninol and -hydroxyphenylalaninol
- 2-amino-1,4-anhydro-pentitol and 3-amino-1,5-anhydro-4-deoxy-hexitol with the arabino configuration
- (S)-4-tosyloxymethyl-2-oxazolidinone, required for the synthesis of protected amino alcohol derivatives
- 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine [(S)-HPMPC]
- chiral building block used to construct an epoxyvinyl iodide intermediate in a synthesis of a furanocembrane, a marine natural product
| [Definition]
ChEBI: (R)-glycidol is a glycidol. It is functionally related to a (R)-1,2-epoxypropane. It is an enantiomer of a (S)-glycidol. | [General Description]
Enantioselective esterification of (R)-(+)-glycidol with n-butyric acid in organic media using hybrid gel-entrapped lipase on Celite has been reported. | [Purification Methods]
[S(-)-isomer, § also available on polymer support, has b 49-50o/7mm, 66-67o/19mm, [ ] D -1 5o(neat)], [R(+)-isomer has b 56 -5 6 . 5o/11mm, d 4 1.117, n D 1.429, [ ] D +15o (neat)]. Purify glycidol by fractional distillation. |
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