772313
4-Methoxyphenyl β-D-glucopyranoside
97%
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About This Item
Empirical Formula (Hill Notation):
C13H18O7
CAS Number:
Molecular Weight:
286.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
Product Name
4-Methoxyphenyl β-D-glucopyranoside, 97%
InChI
1S/C13H18O7/c1-18-7-2-4-8(5-3-7)19-13-12(17)11(16)10(15)9(6-14)20-13/h2-5,9-17H,6H2,1H3/t9-,10-,11+,12-,13-/m1/s1
SMILES string
COc1ccc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1
InChI key
SIXFVXJMCGPTRB-UJPOAAIJSA-N
assay
97%
form
solid
mp
133-172 °C
storage temp.
2-8°C
Quality Level
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
涉药品监管产品
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G M Aerts et al.
Biochimica et biophysica acta, 660(2), 317-324 (1981-08-13)
The interaction of alcohols in the hydrolysis of aryl beta-D-glucopyranosides and aryl beta-D-xylopyranosides by beta-D-glucosidase (beta-D-glucoside glucohydrolase, EC 3.2.1.21) from Stachybotrys atra has been investigated. The results constitute support for the presence of a glycosyl-enzyme intermediate, formed during the first
Z Zhang et al.
Carbohydrate research, 295, 41-55 (1996-12-13)
p-Methoxyphenyl (pMP) beta-D-glycopyranosides (Glc, Gal, GlcNPhth, GalNPhth, GlcNTroc, Gal beta 4Glc, Gal alpha 4Gal) were prepared from the corresponding 1-O-acetyl sugars in 79-90% yield, using boron trifluoride etherate as promoter. Treatment of the pMP glycosides with acyl chlorides or bromides
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