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Tri-O-acetyl-D-galactal, 98%|106650|4098-06-0

Tri-O-acetyl-D-galactal, 98%

Cat. No JK106650_5_G
J&K Chemical

Product Information

Product Name
Tri-O-acetyl-D-galactal, 98%
Brand Name
J&K
Product Number
106650
CAS
4098-06-0
Molecular Formula
C12H16O7
Molecular Weight
272.25
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
640125
IUPAC Name
(2R,3R,4R)-3,4-diacetyloxy-3,4-dihydro-2H-pyran-2-ylmethyl acetate
InChI Key
LLPWGHLVUPBSLP-IJLUTSLNSA-N
SMILES
CC(=O)OCC@@H1C@@H(C@@H(C=CO1)OC(=O)C)OC(=O)C

Properties

Melting Point
34-38
Optical Activity
-22.0°to -17.0°(C=3, CHCl3)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H317
H319
Precautionary Statement
P261
P272
P280
P321
P501
P302+P352
P333+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
Storage Condition
Store at 2-8℃

References

Ferrier Glycal Allylic Rearrangement
Publication Name: Namensreaktionen
Publication Date: 2024
DOI: 10.1007/978-3-031-52850-7_51

Intermolecular CuAAC Click Conjugation of Carbohydrates
Publication Name: Science of Synthesis
Publication Date: 2021

Effects of lipophilicity, protecting group and stereochemistry on the antimalarial activity of carbohydrate-derived thiochromans
Publication Name: Medicinal Chemistry Research
Publication Date: 2018-01-03
DOI: 10.1007/s00044-017-2105-5

Recent Functionalizations of Primary Sulfonamides
Publication Name: Synthesis
Publication Date: 2016-07-19
DOI: 10.1055/s-0035-1562503

Synthesis of 2,3-Unsaturated Alkynyl O-Glucosides from Tri-O-acetyl-d-glucal by Using Montmorillonite K-10/Iron(III) Chloride Hexahydrate with Subsequent Copper(I)-Catalyzed 1,3-Dipolar Cycloaddition
Publication Name: Synthesis
Publication Date: 2015-08-13
DOI: 10.1055/s-0034-1378829

Tri-O-acetyl-D-galactal, 98%

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