| Identification | Back Directory | [Name]
(1S,5R)-(-)-2-OXABICYCLO[3.3.0]OCT-6-EN-3-ONE | [CAS]
43119-28-4 | [Synonyms]
(1S,5R)-2-OXABICYCLO[3.3.0]OCT-6-EN-3-ONE
(-)-CIS-2-OXABICYCLO[3.3.0]OCT-6-EN-3-ONE
(1S,5R)-2-Oxabicyclo[3.3.0]oct-6-en-3-one 99%
(1S,5R)-(-)-2-OXABICYCLO[3.3.0]OCT-6-EN-3-ONE
(1S,5R)-2-Oxabicyclo[3.3.0]octane-6-ene-3-one
(1β,5β)-2-Oxabicyclo[3.3.0]octane-6-ene-3-one
(1S,5R)-2-Oxabicyclo[3.3.0]oct-6-en-3-one, >=99%
(1S,5R)-(-)-CIS-2-OXABICYCLO[3.3.0]OCT-6-EN-3-ONE
(1S,5R)-(-)-cis-2-Oxabicyclo[3.3.0]oct-6-en-3-one,97%
(3AR,6AS)-3,3A,6,6A-TETRAHYDRO-2H-1-OXAPENTALEN-2-ONE
(3aR,6aS)-3,3a,6,6a-tetrahydrocyclopenta[b]furan-2-one
(1S,5R)-(-)-CIS-2-OXABICYCLO[3.3.0]OCT-6- EN-3-ONE 97%
(3AR,6AS)-3,3A,6,6A-TETRAHYDRO-2H-CYCLOPENTA[B]FURAN-2-ONE
2H-Cyclopenta[b]furan-2-one,3,3a,6,6a-tetrahydro-, (3aR,6aS)-
(3aR,6aS)-3,3a,6,6a-Tetrahydro-2H-cyclopenta[b]furan-2-one, (3aR,6aS)-3,3a,6,6a-Tetrahydro-2H-1-oxapentalen-2-one | [EINECS(EC#)]
610-106-4 | [Molecular Formula]
C7H8O2 | [MDL Number]
MFCD00010402 | [MOL File]
43119-28-4.mol | [Molecular Weight]
124.14 |
| Chemical Properties | Back Directory | [Appearance]
white to beige or brownish crystalline powder | [Melting point ]
44-46 °C(lit.)
| [Boiling point ]
263.1℃ | [density ]
1.196 | [refractive index ]
1.4906 (estimate) | [Fp ]
104.0℃ | [storage temp. ]
0-6°C | [solubility ]
DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2) (1:2): 0.33 mg/ml,Ethanol: 15 mg/ml | [form ]
A crystalline solid | [color ]
Off-white to light yellow | [Optical Rotation]
[α]22/D 103°, c = 1 in methanol | [BRN ]
3537516 | [InChI]
InChI=1S/C7H8O2/c8-7-4-5-2-1-3-6(5)9-7/h1-2,5-6H,3-4H2/t5-,6-/m0/s1 | [InChIKey]
RYBPGUMSFWGGLP-WDSKDSINSA-N | [SMILES]
O1C(=O)C[C@]2([H])C=CC[C@]12[H] |
| Hazard Information | Back Directory | [Chemical Properties]
white to beige or brownish crystalline powder | [Uses]
(?)-G-Lactone is a synthetic intermediate useful for prostaglandins synthesis[1]. | [References]
[1] Alphand, V, et al. Microbial Transformations 16. One-step synthesis of a pivotal prostaglandin chiral synthon via a highly enantioselective microbiological Baeyer-Villiger type reaction. Tetrahedron Lett. 30(28), 3663-3664 (1989). |
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