J66442 2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone, 97+%
Numéro de CAS
30725-00-9
Synonymes
2,3-O-Isopropylidene-D-ribonic acid y lactone
2,3-O-Isopropylidene-D-ribonolactone
FDS
| Stock No. | Conditionnement | Prix ($) | Quantité | Disponibilité |
|---|---|---|---|---|
| J66442-ME | 500mg | 25,10 |
|
|
| J66442-03 | 1g | 33,00 |
|
|
| J66442-06 | 5g | 130,00 |
|
|
2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone, 97+%
MDL
MFCD00080793
Propriétés chimiques
Formule
C8H12O5
Poids moleculaire
188.18
Forme
Powder
Point de fusion
135-138°
Storage & Sensitivity
Ambient temperatures.
Solubilité
Soluble in methanol at 50mg/ml, acetone, dichloromethane, ethyl Acetate.
Applications
2,3-O-Isopropylidene-D-ribonic acid-1,4-lactone is used for the synthesis of C-nucleosides, prostanoids and GABA analogs via homochiral 2-piperidones. It is the starting material for the preparation of biochemical compounds including C-nucleosides, such as neplanocin A, and GABA analogs, via homochiral 2-piperidones.
Notes
Soluble in methanol at 50mg/ml
Références bibliographiques
Kotohiro Nomura and Richard R. Schrock.Preparation of Sugar-Coated Homopolymers and Multiblock ROMP Copolymers. Macromolecules.1996, 29, (2), 540-545.
Amélia P. Rauter; José Figueiredo; Maria Ismael; Tana Canda; Josep Font; Marta Figueredo. Efficient synthesis of α,β-unsaturated γ-lactones linked to sugars. Tetrahedron: Asymmetry.2001, 12, 1131-1146.
Autres références
Beilstein
10090
Code tarifaire harmonisé
2932.99
TSCA
No
Produits chimiques
Sciences de la vie
Métaux et matériaux
Catalyseurs
