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1,2-O-Isopropylidene-α-D-glucofuranose, 98%|149156|18549-40-1

1,2-O-Isopropylidene-α-D-glucofuranose, 98%

Cat. No JK149156_5_G
J&K Chemical

Product Information

Product Name
1,2-O-Isopropylidene-α-D-glucofuranose, 98%
Brand Name
J&K
Product Number
149156
CAS
18549-40-1
Molecular Formula
C9H16O6
Molecular Weight
220.22
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
87704
IUPAC Name
(1R)-1-(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro2,3-d1,3dioxol-5-ylethane-1,2-diol
InChI Key
BGGCXQKYCBBHAH-OZRXBMAMSA-N
SMILES
CC1(OC@@H2C@H(C@H(OC@@H2O1)C@@H(CO)O)O)C

Properties

Melting Point
156
Optical Activity
-13° to -11° (C=1, H2O)

Safety Information

Precautionary Statement
P262

References Data Source From Pubchem

Sources of hepatic glycogen synthesis in mice fed with glucose or fructose as the sole dietary carbohydrate
Publication Name: Magnetic Resonance in Medicine
Publication Date: 2018-07-29
DOI: 10.1002/mrm.27378

A Short Asymmetric Synthesis of Sauropunols A–D
Publication Name: Synthesis
Publication Date: 2017-04-18
DOI: 10.1055/s-0036-1588999

Synthesis of Secondary Metabolites from Higher Fungi
Publication Name: Synthesis
Publication Date: 2015-09-09
DOI: 10.1055/s-0034-1378774

Scaling-up the synthesis of myristate glucose ester catalyzed by a CALB-displaying Pichia pastoris whole-cell biocatalyst
Publication Name: Enzyme and Microbial Technology
Publication Date: 2015-07
DOI: 10.1016/j.enzmictec.2015.04.002

2H enrichment distribution of hepatic glycogen from2H2O reveals the contribution of dietary fructose to glycogen synthesis
Publication Name: American journal of physiology. Endocrinology and metabolism
Publication Date: 2013-02-15
DOI: 10.1152/ajpendo.00185.2012

1,2-O-Isopropylidene-α-D-glucofuranose, 98%

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