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772313

Sigma-Aldrich

4-Methoxyphenyl β-D-glucopyranoside

97%

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About This Item

Empirical Formula (Hill Notation):
C13H18O7
CAS Number:
6032-32-2
Molecular Weight:
286.28
MDL number:
MFCD06797143
UNSPSC Code:
12352201
PubChem Substance ID:
329767554
NACRES:
NA.22

Assay

97%

form

solid

mp

133-172 °C

storage temp.

2-8°C

SMILES string

COc1ccc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1

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

InChI key

SIXFVXJMCGPTRB-UJPOAAIJSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

772313-BULK:
772313-VAR:
772313-5G:
772313-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBN7426V

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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
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

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