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1,2,3,4,6-Penta-O-acetyl-D-mannopyranose, 98%|334526|25941-03-1

1,2,3,4,6-Penta-O-acetyl-D-mannopyranose, 98%

Cat. No JK334526_25_G
J&K Chemical

Product Information

Product Name
1,2,3,4,6-Penta-O-acetyl-D-mannopyranose, 98%
Brand Name
J&K
Product Number
334526
CAS
25941-03-1
Molecular Formula
C16H22O11
Molecular Weight
390.34
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11811209
IUPAC Name
(2R,3R,4S,5S)-3,4,5,6-tetraacetyloxyoxan-2-ylmethyl acetate
InChI Key
LPTITAGPBXDDGR-WHWZVRATSA-N
SMILES
CC(=O)OCC@@H1C@H(C@@H(C@@H(C(O1)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C

Properties

Melting Point
68
Optical Activity
+51° to +57° (C=1, CHCl3)

Safety Information

Precautionary Statement
P262
Storage Condition
Store at 0℃

References Data Source From Pubchem

Tobramycin-loaded complexes to prevent and disrupt Pseudomonas aeruginosa biofilms
Publication Name: Drug Delivery and Translational Research
Publication Date: 2021-11-28
DOI: 10.1007/s13346-021-01085-3

Synthesis of 3-deoxy-2-uloses via the indium-mediated allylation reaction
Publication Name: Monatshefte für Chemie - Chemical Monthly
Publication Date: 2019-05-02
DOI: 10.1007/s00706-019-02438-y

Sulfonated carbon nanocage as a catalyst for the per-O-acetylation of carbohydrates
Publication Name: Kinetics and Catalysis
Publication Date: 2014-03
DOI: 10.1134/s0023158414020037

Synthesis and characterisation of novel glycoclusters based on cell penetrating heptakis(6-aminoethylamino-6-deoxy)-β-cyclodextrin
Publication Name: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Publication Date: 2010-09-01
DOI: 10.1007/s10847-010-9840-2

Synthesis of a derivative of a pentasaccharide repeating unit of the O-antigenic polysaccharide of the bacterium Klebsiella pneumoniae O3 as a benzoylated 2-methoxycarbonylethyl thioglycoside
Publication Name: Russian Chemical Bulletin
Publication Date: 2009-02
DOI: 10.1007/s11172-010-0033-3

1,2,3,4,6-Penta-O-acetyl-D-mannopyranose, 98%

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