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About This Item
Empirical Formula (Hill Notation):
C8H15NO4
CAS Number:
Molecular Weight:
189.21
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
3588654
MDL number:
biological source
Castanospermum australe seeds
product line
BioUltra
assay
≥94% (GC)
form
powder
mp
212-215 °C (dec.)
solubility
1 M HCl: 20 mg/mL, clear, colorless to faintly yellow
storage temp.
2-8°C
SMILES string
O[C@H]1CCN2C[C@H](O)[C@@H](O)[C@H](O)[C@@H]12
InChI
1S/C8H15NO4/c10-4-1-2-9-3-5(11)7(12)8(13)6(4)9/h4-8,10-13H,1-3H2/t4-,5-,6+,7+,8+/m0/s1
InChI key
JDVVGAQPNNXQDW-TVNFTVLESA-N
Biochem/physiol Actions
α-glucosidase Inhibitor
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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K S Ajish Kumar et al.
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The utility of a D-glucose-derived aziridine carboxylate was demonstrated for the synthesis of polyhydroxylated quinolizidine and indolizidine alkaloids. The chemoselective reduction of 1 followed by two-carbon homologation by the Wittig reaction afforded gamma,delta-aziridino-alpha,beta-unsaturated ester 9, which on regioselective nucleophilic aziridine
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[reaction: see text] An asymmetric total synthesis of (-)-swainsonine and (+)-6-epicastanospermine is described from a common intermediate, which is obtained through diastereoselective [2 + 2] cycloaddition of dichloroketene to a chiral enol ether.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C3784-1MG | 04061833486382 |
| C3784-5MG | 04061833269817 |