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关于此项目
经验公式(希尔记法):
C8H15NO4
化学文摘社编号:
分子量:
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
存储类别
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
法规信息
新产品
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相关内容
Product Information Sheet
Julien Ceccon et al.
Organic & biomolecular chemistry, 7(10), 2029-2031 (2009-05-08)
An asymmetric synthesis of (+)-castanospermine is presented in which enol ether metathesis-hydroboration/oxidation is used for stereoselective installation of the trans-trans hydroxyl groups on the piperidine ring of the alkaloid.
Thomas Jensen et al.
The Journal of organic chemistry, 74(22), 8886-8889 (2009-10-28)
A nine-step synthesis of (+)-castanospermine has been accomplished in 22% overall yield from methyl alpha-D-glucopyranoside. The key transformations involve a zinc-mediated fragmentation of benzyl-protected methyl 6-iodoglucopyranoside, ring-closing olefin metathesis, and strain-release transannular cyclization to afford the indolizidine skeleton of the
Tomohisa Kato et al.
Analytical biochemistry, 405(1), 103-108 (2010-06-24)
Saccharide primers, such as dodecyl beta-lactoside (Lac-C12), are unique artificial precursors of glycolipid synthesis. In culture media supplemented with saccharide primers, they are taken up by the cells in the culture media and glycosylated by cellular glycosyltransferases in the Golgi
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| C3784-1MG | 04061833486382 |
| C3784-5MG | 04061833269817 |