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(−) -G-Lactone

CAT: 0013-GTR19232421-03Size: 1 gDry Ice: NoHazardous: No
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CAT#:0013-GTR19232421-03Size:1 g
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Description
(–) -G-lactone is a chiral bicyclic γ-lactone synthesized via asymmetric Baeyer-Villiger oxidation. It serves as a key synthon in prostaglandin synthesis and has been employed as a building block for HIV-1 protease inhibitors in medicinal chemistry research.
CAS Number
43119-28-4
Smiles
O=C1C[C@@H]2C=CC[C@@H]2O1
Molecular Formula
C7H8O2
Molecular Weight
124.139
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

(3aR,6aS)-3,3a,6,6a-tetrahydro-2H-cyclopenta(b)furan-2-one
CAS Number43119-28-4
PubChem CID643405
IUPAC Name(3aR,6aS)-3,3a,6,6a-tetrahydrocyclopenta[b]furan-2-one
Molecular FormulaC7H8O2
Molecular Weight124.14
XLogP0.8
Topological Polar Surface Area26.3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Heavy Atom Count9
Formal Charge0
Complexity172
SMILES
C1C=C[C@@H]2[C@H]1OC(=O)C2
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
Chemical Structure
2D Structure
2D structure of (3aR,6aS)-3,3a,6,6a-tetrahydro-2H-cyclopenta(b)furan-2-one
CAS: 43119-28-4
CID: 643405
Formula: C7H8O2
MW: 124.14
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight124.14
XLogP30.8
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass124.052429494
Monoisotopic Mass124.052429494
Topological Polar Surface Area26.3 Ų
Heavy Atom Count9
Formal Charge0
Complexity172
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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CatalogName
T85030-01(−) -G-Lactone
OR1034367-01(-) -G-Lactone
G00190-01D-Galactono-g-lactone
G05730-01L-Gulonic-g-lactone
H01540Heptanoic-g-Lactone 95%
R01830-01D- (+) -Ribonic acid g-lactone
G05725-01D-Gulonic-g-lactone 99%
H161064-Hydroxynonanoic acid-g-lactone
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